A Material Safety Data Sheet (MSDS) https://liquetax.com/page%20information/material-safety-data-sheet-msds-certificate.htmlis a critical document that provides detailed information on the properties, handling, storage, and emergency measures related to hazardous chemicals. It is an essential tool for ensuring workplace safety and regulatory compliance.
Meterial Sefty Data Sheet(MSDS), MSDS Registration, Meterial Sefty Data Sheet (MSDS) registration by Liquetax,
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I want to start by saying, I am not asking for money or a place to stay or anything. I just really want every entity, whether it's political, governmental, charitable, legal, or journalistic, and every individual who cares about solving homelessness to hear my story. I believe many others are experiencing the same trampling of rights and failure of enforcement that I am. So, even if you're someone who can't help me, I still want to make you aware, because this is life or death for many of us. Feel free to forward to anyone you think could assist me in my fight (legal, media, political, etc) or would simply benefit from awareness.
For me, a US citizen with 2 college degrees earned in 4 years, and who worked 2-3 jobs most of my life (and who has made an effort to live my life as if John Quinones might show up with a tv crew), I am finding survival near impossible, and it seems Karma is having gotten lost on it's way back to me. I say this because I can't imagine someone with less experience, abilitly, access, or education having to deal with the complete inability, and often unwillingness, of LAHSA (and it's subcontractors) to do what LAHSA themselves prescribed as their plan for Rapid Rehousing of the homeless.

short story: (sort of):

LAHSA Grievance Coordinator completely ignored all evidence allowing a service provider to leave me in peril after improper exiting, breach of contract, complete failure to meet LAHSA's required service standards; and in debt after consistently late payments and related fines, shorted rental payments accrued over the past year, and zero disbursement of other prescribed assistance.
I was told that I would have rent up to $1600 paid by First to Serve. I went out of my way to find and get approved for an affordable unit (originally $698, now $800). My case manager did not help me at all. I did everything myself, and I paid for everything myself. I secured the apartment, cleared it with HCIDLA, paid app fee, paid a co-signer service, paid for Emotional Support letter from online doc, paid U-haul, moved it all myself. I furnished my apartment from the dumpsters (the used bed and mattress they supposedly ordered from Goodwill never arrived), where I got even sheets and towels, and cookware.
I've never received the following financial provisions: application assistance, moving expenses, move-in expenses (furniture allowance, etc.), utility assistance, car repair assistance (car has needed simple repairs for a year), car registration help, help with storage expenses, etc. These provisions are not optional, but required, according to LAHSA program standards and contracts with service providers.
I also never received any case management (they're supposed to have monthly in-home visits to make sure I'm on track to be financially sufficient. I haven't had a single one in 2 years), or supportive services (help with getting treatment for medical issues or mental health issues, domestic violence support, job assistance, goal planning, etc.). I never even received paperwork or info about the program.
LAHSA Grievance Coordinator took 5 months to begin the investigation (their web page says it takes 5 days to complete a grievance!), and one month to complete the investigation (without a single meeting or phone conversation with me). After all this, her decision was nothing more than restating every false claim FTS made, despite the preponderance of evidence I sent her from the very beginning. She never asked me any questions nor allowed me a chance to clarify any item.
Now I will lose my home and everything in it, leaving me on the streets with health problems and 2 dogs. I have had to shelve my work on the small businesses I was trying to make profitable, postpone medical appointments, and basically put all my efforts towards prolonged survival on hold while I scramble to get someone to help me save my home (and life), sending out emails and obsessively researching the legality of what is being done and the options I have (which are hopeless). I KNOW MY RIGHTS, BUT NO ONE IS WILLING TO ENFORCE THEM FOR ME.

long story:

I was homeless due to a domestic violence situation and I completed Project Roomkey, followed by Rapid Re-housing in an affordable unit. I received a 3 day notice on the evening of October 11 and when I asked my Rapid Rehousing provider (First to Serve) why they hadn't paid rent, I was informed they exited me from the program. My case manager claims I was warned in advance by email, but they never emailed me.
I know First to Serve is contracted by LAHSA to provide rapid rehousing with very specific services and assistance and they signed same contract with me (though I've never received a copy of it, despite multiple requests). They have failed to meet LAHSA minimum standards almost entirely in my case. I was told that I would have a rent up to $1600 paid by First to Serve. I went out of my way to find and get approved for an affordable unit for originally $698. My case manager did not help me at all. I secured the apartment, cleared it with HCIDLA, paid app fee, paid a co-signer service, paid U-haul, moved it all myself. I furnished my apartment from the dumpsters (the used bed and mattress they supposedly ordered from Goodwill never arrived), even sheets and towels, and cookware. I've never received the following financial provisions: application assistance, moving expenses, move-in expenses (furniture allowance, etc.), utility assistance, car repair assistance (car has needed simple repairs for a year), car registration help, storage expenses. Also, they've shorted rent payments since December and racked up unpaid late fees every month since April, which they haven't paid, and never paid for broadband which is required part of rent.
I also have not received any case management. They're supposed to have monthly in-home visits to make sure I'm on track to be financially sufficient. I haven't had a single one in 2 years. I haven't even gotten phone calls to check on me. I only heard from them when I was begging them to pay rent (and sometimes not even then). Half the time I didn't even have a case manager. These are not guidelines. These are legally binding contracted requirements. I am a pro at research, so I've found all the paperwork detailing program standards. I often say "knowing your rights is useless, if no one enforces them." My case manager insisted that I "had 2 years to get a job." And I said "I can't with long covid pain and brain problems." I have an incredibly debilitating case of Long Covid (see footnote to understand the extent of my symptoms). She claims I never told them my health problems, which of course I have email proof of telling them, multiple times. I've been trying to get a diagnosis so I could get temporary disability until some treatment is offered, but it's been a battle finding a Medicaid doctor who acknowledges that Long Covid is not mental, let alone has any clue how to treat it. After 2 years I settled for one who at least listened to my symptoms, didn't blame them on a heart condition I've had since age 11, and didn't hit on me (like the first doc). I've had to shelve the quest for diagnosis to focus on the battle to save my home.
I created 5 small businesses while in Project Roomkey, and I'm working hard towards getting them profitable. It has been a struggle with the brain fog, memory loss, lack of focus, insomnia, and chronic pain. I dumpster dive and sell what I find to feed my dogs. The constant anxiety and battling to get my rent paid (got 3 day notices multiple times) definitely hindered my ability. Every time I work on my businesses I feel guilty and think I should focus on housing. And vice versa. I feel like I'm wrong no matter what, leaving me in a constant state of helplessness (a feeling I never even had a passing whiff of my entire life, even when in DV situation! I'm just starting to get some minor relief from the Long Covid symptoms thanks to my own research and self-medicating with supplements like magnesium and 5-MTHF (though doc spotted a scar on heart x-ray that needs further examination).
The case manager (7th by the way) proceeded to tell me I should just ride out an eviction here and then go to a shelter. I don't want an eviction on my record. And I will die if I lose this place. I literally lose everything. I won't even be able to put stuff in storage. And my car is still dead, so I'd lose that too. I'd have my dogs and whatever I could carry, and nowhere to go. And who knows if my heart will give out. I'm still fighting to get FTS to pay what they owe, but they deny owing anything and claim I received all services, ignoring the official ledger from my landlord, and all my documented proof.
I literally have proof of everything- every call, every email, every text, every shorted payment, my health issues, and my attempts at getting help. FTS sees nothing wrong with leaving me an unpaid balance of shorted rent payments and unpaid late fees (~$1000) accrued while ON the program, nor with leaving me worse than they found me. I need to find work now that I'm starting to feel capable, and/or focus on making my businesses profitable, and/or get back on a housing program with a provider who will provide me what I was entitled to. I have so much trouble starting any task because I fear prioritizing the wrong goal and am paralyzed by anxiety and guilt (for failing my dogs). First to Serve failed me every step of the way and set me up for failure. And then LAHSA pried my fingers off the ledge, not to lift me up, but to push me off.
I have no family left and no friends that can help. I want so badly to work hard and support myself. I earned 2 college degrees in 4 years and worked up to 3 jobs most of my life, eventually as a GM of a barestaurant. I only ended up homeless because of a domestic violence situation 1 month before the pandemic hit (which they also offered me no support for, which would have helped as I have PTSD from the abuse and 2 attempts on my life by strangulation). I'm a good person who helped the homeless even while homeless. Even now, I dumpster dive for blankets and clothes that I wash and distribute to local homeless. I feed local homeless meals made from any surpluses from the food pantry. My motto is Survive then Thrive, then help others, but I fear I might not survive.
I just need someone to do right by me, and not for much longer. LAHSA Grievance restated every false claim FTS made, despite the preponderance of evidence I sent her. Now I will lose my home and everything in it, leaving me on the streets with health problems and 2 dogs. I know my rights, but no one is willing to enforce them for me. You're welcome to forward my story to anyone who could help me fight to get LAHSA to provide me what I was denied, or to anyone who coulld bring more attention to my story. I want to save me and my dogs, but I will not pull the ladder up behind me.. I want to make sure no one else suffers due to this systemic inadequacy and corruption.
Thank you,
Carolanne Burtchell
*LONG COVID as a disability
🔸I have diminished breathing capacity. I used to hike 6 miles with my dogs, now I’m winded after walking 2 blocks, or even just tying my shoes. Covid leaves what looks like shattered glass in your lungs. It may go away, it may not. I’m not a smoker, yet I’m breathing like I chain-smoked for years. When I return from walking my dogs, I am overheated, dizzy, and nauseous. It feels like I’m going to have a heart attack.
🔸I have serious insomnia. I sleep maybe 4 hours a night, often not at all. The next day when I try to work on my computer, I am narcoleptic and sometimes fall face-first into laptop. Even if not sleepy, I am unable to focus. I feel like I just got ADHD. It takes me epic lengths of time to do tasks I found simple prior.
🔸I am achy all the time. My back, my neck, shoulders. All my muscles hurt no matter how I sleep. Standing hurts one set of muscles. Sitting hurts another. Lying down hurts another. I’m basically never comfortable. I’m constantly stretching to try to feel less pain but then that leads to cramps or twitches. I also get unexplained stabbing pains in feet.
🔸 I get an anaphylactic episode almost every day for about an hour. It happens with no trigger. It’s like a coating fills my throat.
🔸I have migraines weekly. Never had them before. I get the full spectrum of symptoms. Even with Excedrin, they’re crippling.
🔸I have severe swelling and edema in my feet and ankles and partway up calf. Its painful and made it difficult to wear shoes or stand up for any length of time. Occasionally I get stabbing pains in feet. The swelling often is joined with bruising, a rash, an itch that never subsides. The skin is being stretched till it breaks and peels. The pressure is painful even when seated. When walking, I cannot bend ankles and struggle to walk my dogs.
🔸I have brain fog. It’s similar to pregnancy brain. I find it hard to focus and even harder to remember (not song lyrics—those are safe lol). My memory is diminished. I’m having trouble accessing vocabulary. My IQ was 156 and now I feel brain damaged.
🔸I already had serious occasional heartburn, but now it’s sooooo much worse. I have it after sipping water or leaning over. It affects me 75% of the month (not sure why I get the 25% break, but I’ll take it. I also get intestinal cramping I never had before.
🔸My eyes are super sensitive to light, esp. computer light. Sucks when all my work is on there now. I have double vision and it feels like my contacts don’t fit right.
🔸I’m itchy, often. Kind of like a junkie between hits. I believe it has to do with the circulation being affected because Covid-19 weakens your veins, sometimes causing them to leak, which in turn causes itching and swelling.
🔸I have chronic fatigue, surely caused by all these symptoms.
🔸My anxiety is through the roof.
🔸 I will say, my sense of smell and taste remain unscathed. Thank God. A bartender with no taste buds can’t create recipes.
🔸 While it hasn’t happened, I read in credible science journals that I can have a blood clot, even a stroke, at any time. That’s terrifying.

Has anyone been able to obtain the safety data sheet for their Vanmoof, usually needed for customs clearance when you are shipping the bike due to the battery? Where can this be found or did you have to ask Vanmoof directly for it?
Context is I am in middle of shipping my Van Moof A5 from the Netherlands to USA and it is currently requiring battery safety forms for the customs check before it continues onwards. Checked Vanmoof websites and don't see anything besides a "Certificate of Conformity" which doesn't look like what is needed.
I did send inquiries to Vanmoof via all their channels (FB Messenger, Instagram, website email form *rolls eyes*) so hoping they actually get back to me. Really sucks there isn't a direct phone number - I haven't had to ask Vanmoof for any support since the bankruptcy so I'm praying they actually will get back to me!

Received a message from a customer asking for a msds sheet for a skincare product. First time encountering so wondering if anyone has any experience with this. Any insight would be greatly appreciated!

I work for a blasting company and we use IBC's for some of our chemicals and I have been looking at them thinking a cube or two would make a wonderful compost bin.
I read the MSDS and it is made from the following: (this information is readily available online as it is a Material Safety Data Sheet, I am not spreading info on how to make it or giving instructions on what to do with it or anything of the sort, this is for information purposes only.)

• ammonium nitrate (aka fertilizer (nitrogen))
  CAS No: 6484-52-2
  30 - 60%
  
• Nitric acid (decomposes to oxides of nitrogen)
  CAS No: 7696-37-2
  0 - <0.5%
  
• Water (aka...... water)
  CAS No: 7732-18-5 (it's water.....)
  30 - 60%
  
• Non Hazardous components
  CAS No: N/A
  0 - 1%
  

Ecotoxicity:
Keep out of waterways. Ammonium nitrate is a plant nutrient. Large scale contamination may kill vegetation and cause poisoning in livestock and poultry. Ammonium nitrate was evaluated at 5, 10, 25 and 50 mg (NH4+)/L. The fertility of Daphnia magna was decreased at 50 mg/L. Post embryonic growth of crustacea was impaired at 10, 25 and 50 mg/L. Can stimulate weed and algal growth in static surface waters.
Now, the container has no liquid in it once we are done with it (as it need to be completely removed prior to discarding) as it is governed by dangerous goods laws for obvious reasons. So it would only have residual stuff left in it.
My main question as the compost was to be used ony veggie garden and going by the SDS it is fine to use, right? Just wanted a second opinion before I pull the trigger.
Edit: manufacturer... Can't edit the title unfortunately
Mods, if there is any issue with the post please reach out to me and I can provide a link to the MSDS or I can remove information as required. I figured as it is publicly available it wouldn't be an issue.

I work for a large company that has to be rather strict with material it uses and making sure everything is disposed of and stored properly. We are trying to get PVA approved for use in the building. Right now our environmental team is hesitant on approving PVA because the only MSDS sheet we can find with a US address and phone number lists methanol on the sheet (European safety sheets don't seem to have it listed). I could use some help finding a US manufacture or distributer who could provide us with an MSDS that would satisfy our environmental team.

Hello everyone,
I am currently on the journey in finding better gel products that have low hema content. I was provided a msds sheet and the top ingredients is Aliphatic urethane acrylates which is at 40%. I saw that hema is at 10%, however, Aliphatic urethane acrylate is an unfamiliar ingredient to me so I am wondering if it is safe. That is all, thank you!

Hello bokashi,
Seeking advice.
Earlier this week - when I found it under my car seat - I was reminded that I purchased a 500ml bottle of EM bokashi liquid... a month or so ago...
So it's been rolling around in my car during an Australian summer (though not the hottest we've ever had) with daily max. and min. temperatures generally between 5C-35C (41F - 95F) and perhaps hitting 40C/104F on a couple of occasions. Factor in the car environment and I have to imagine that it likely repeatedly hit above 50C, and at times maintained those temps for many hours.
The product Material Safety Data Sheet states:

Conditions to avoid: Excessive direct sunlight temperatures above 50C may damage product

I am yet to open the bottle. It didn't burst or leak so that's something, but I have no idea whether the EMs are still alive, and/or in what ratios.
So,

• Is it possible to "reinoculate" it to bring it back to life?
• Should I experiment by using it as a "starter" with the 5%5%90% starter, molasses, water method to see if it grows anything?
• What other method? ingredients? ratios? would you suggest to recover this EM liquid.

Thanks!
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Hi everyone, hope you had a good session. As promised, the spreadsheet has evolved to cover all Masters by CU online.
MSCS Sheet: https://tinyurl.com/cu-boulder-mscs MSCS Review Form: http://tinyurl.com/cu-mscs-review MSDS Sheet: https://tinyurl.com/cu-boulder-msds MEEM Sheet: https://tinyurl.com/cu-boulder-meem MSEE Sheet: https://tinyurl.com/cu-boulder-msee MSDS/MEEM/MSEE Review Form: http://tinyurl.com/cu-elective-review
Hope everyone can contribute by commenting course information to the courses you have taken in each info sheet and submitting a review form for it.

Subject: Seeking Advice on Persistent Nasal Mucus Production and chronic pain.
Hello AskDocs,
I hope this community can provide some insights or suggestions regarding a persistent health issue I've been dealing with for quite some time. I'm a 19-year-old individual who has been experiencing chronic symptoms for the past 12 years.
Notable information that may or may not be related to the post.

• Was advised to take hormone shots when younger, I was at the time afraid of needles (not vaccinations) and wasn't convinced by parent to pursue the treatment. Their reasoning was my parents were short, so I'd likely be as well.
  
• During the start of my daily chronic migraines, the school tried to keep me in school attending as much days as possible, which is fine as studdies show it's beneficial and insert 50 other reasons here. However to do so, the nurse gave me Excedrin migraine (extra strength) which at the time had caffeine, an nsaid + acetaminophen. I was given multiple of these pills a day at the highest dosage. Then with the migraines not improving, I got a ped neurologist, they ran through the usual testing, usual first line medications, then there was nothing left. They esentially said there's nothing they can do with the current limitations of pediatrics, at the time not even botox was allowed. I was homebound from school from the pain being so severe, the lights and sound was too much. The kids being so loud and the type of lights they use. The ped neuro was back and forth between either keeping me on homebound, or removing it entirely, as in, they literally one month had me on homebound, then the next expected every single day for me to attend. One year they had me entirely on homebound, then the last month of school I wasn't.. extremely odd ways to coax someone back into an environment, but that's unrelated. The neuro seemed to think regardless of the pain that I should attend school everyday. The school ended up calling the neuro.. (yes, an educational system with no medical expertise) they said they believed it was in my best interest to not be on homebound. My mom at the time, fought both of them, and we ended up going to court for truency, which resulted in us winning. The neuro gave up esentially.. every appointment was essentially saying I need to drink water and go to school and my pain will go away. This may seem exhaggerated, but it's exactly what was said. She even at one point brought in a med student and said if I won't listen to her about it, then a second opinion saying exactly what she said would make a difference. At one point I was so frustrated when I was a child I was crying/yelling during an appointment about how I've tried everything for pain relief, the water, all of the medications, and it causes so much pain to be put through what I was put through, that going to school with the migraines not being fixed will only cause me more pain. I kid you not, after the session, she listed in my profile that I have a tendency of truancy, behavioral issues, and **neglect**.
  

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• They also prescribed 30 triptans a month, by giving 15 and saying to either cut it in half or just take it every other day. I won't go into semantics on why that's not a good idea by any means, I can guarantee these actions resulted in some sort of moh (rebound). I only found out of the affects of moh and rebounds when I was 16-17, I went cold turkey on all pain relief meds for a year. Nowadays I limit any abortive (triptans, pain relief, or anything related to pain reduction) to 4 times a month max, with the obvious daily migraine prevention medications.

Duration and Frequency:
Since the age of 7, after a severe viral infection, I have been dealing with daily chronic migraines, tinnitus, and an unusual symptom of nonstop nasal mucus production. I haven't gotten a single day of relief from the pain, as in total reduction. I quite literally don't remember what not being in pain feels like, the though of it seems impossible.. and for the longest time from 7-13 I thought the pain was normal, until I spoke up about it. The mucus appears as giant globs, primarily white in color, and is significant enough to cover sheets of tissue paper. This occurs multiple times a day and has been a consistent issue for the past decade.
Attempts at Relief:
I've sought medical attention and have seen an ENT specialist who conducted a nasal examination with a camera, which came back normal. I've tried every first and second line treatment for migraine, lifestyle changes. Beta blockers, calcium channel blockers (as niche as it is), gabapentin, other antiseizure meds for migraine, all cgrp meds, botox, propanolol, co-q10, b12, feverfew, butterbur.. I think you get the point. Any niche or first line prescription or remedy for daily migraines I've tried. Good sleep hygeine, different shades of glasses (fl-41 tint), changing the kelvin of all lights in my house to a frequency that's comftorable for migraine paitents. For my nose, various interventions have been tried, including corticosteroid and antihistamine nasal sprays, a neti pot, and over-the-counter remedies. Unfortunately, these interventions have not provided significant relief.
My current medications with dosages are: propanolol xr 80mg, vyvanse 60mg, vilazodone 40mg, daily vitamin, fish oil, co-q10, b12, b2, d3
Testing: I quite literally asked my PCP to run every single blood test, may be seen as excessive yes, but my insurance covered it. B complex, bmp, cmp, cbc, crp, sed rate, blood sugar levels, hormone testing for a potential imbalance, I tested every vitamin that's possible, fat soluble, got genetic testing done. EKG, sleep study, ct scan.. probably missing more. Nerve blocks can be a hit or miss, I get it with botox as well, they sometimes provide relief, but it always reduces the pain, the numb feeling is a lifetime better than what it usually is. I get either bi yearly or yearly mris, all so far have came back normal besides 1 when I was 8. The notes said there was a "flair" at a certain location and to comeback in x amount of time for another test, the following test it was resolved and unremarkable.
Impact on Daily Life:
The mucus production has led to persistent nasal congestion, making it difficult for me to breathe through my nose during the day and at night. As a result, I've resorted to mouth breathing, impacting my quality of life. Additionally, the mucus turns yellow and burns when I'm about to be sick, serving as an unusual early warning sign. It also requires a lot of force for it to come out of my nose, without expelling it every few hours I cannot breathe out of my nose. During a discharge it sometimes makes a loud sound, or my eardrums pop. My daily migraines have led me to a life that's similar to those during covid, yet that's my reality for the last 12 years.. I'm in a remote college but even that is hard as it is, I exercise and try to prioritize anything proven to provide relief, cbt, I've tried cefaly, nerivo for migraines.. I have a diy migraine cap that I made, I bought these migraine gel strips in bulk from a manufacturer, a few hundred, similar to those u can find at cvs or a drugstore for fever relief, it slightly takes the edge off since I store it in the freezer and the cold somewhat masks the pain, but it's not enough to still be able to function and reacclimate into society.
Concerns and Seeking Guidance:
I'm reaching out to this community to seek any insights, suggestions, or similar experiences that might shed light on the potential causes of these symptoms. Unlikely, but could there be underlying issues that haven't been explored, or are there alternative treatments that I should consider? I'm at the point of where I'd go out of network (I have Medicaid) into debt, or even try an experimental treatment/clinical study, or even pay for a provider or treatment that would provide relief. A literal quarter of my entire life has been taken from me.. and half of the most active time of my life. I want to be able to go outside, or even have the choice to do sports, enjoy time out with my fiance without planning around my pain, just have a shred of normalcy while I'm still young.
I understand that this platform doesn't substitute professional medical advice, but any guidance or shared experiences would be greatly appreciated. If there are specific tests or specialists that I should consider consulting, please let me know.
Thank you in advance for any assistance you can provide. I'm eager to gather information that may help me address these persistent health challenges.

I'm wondering if I could invent a job as a Corporate Dining Service Consultant. Hear me out: My strengths are in organizing a kitchen environment and streamlining processes thereby making what you need to accomplish in the kitchen easier. (Please don't think I'm thinking I'm all that...I just love to make things run better and I think I'm pretty good at it.)
I have done this at every job I've ever worked at; example: making production sheets that actually reflect what is produced by job area or shift. I've organized sheet to shelf inventory systems and order guides. I make closing checklists and deep cleaning task lists for each shift and position. I've made training manuals for each position which include servers, cooks, prep, utility, as well as photographs and descriptions of the standards expected by each position. I just finished working on a tray tag system for my current memory care facility which enables the cook the plate the correct meal and the caregiver to easily identify the resident to serve the residents. I've also done a cheat sheet for State Inspections for each position so when the State walks in, we each know what we need to do as well as organize the temp logs, MSDS sheets and equipment maintenance schedules.
Every time I bring on a new team member and I train them, I'm told that I have made learning the job so much easier and I'm very organized and it helps them a lot. I hear a lot about how many food service directors are very disorganized and run out of food, don't have the correct tools, don't know how to communicate etc.
So I wonder if there is a market for people to pay me to come in, spend a month or so with the company and see how it works and help to make improvements. I know I'd have to avoid stepping on toes, but I wonder if there's a job like that out there or places who would be able to use my skills. What thinks you, Reddit?

Long story short, I live abroad and ordered a Vision Pro for a pickup in store, my friend is picking it up and shipping it internationally via UPS,
Here is the problem UPS are asking for something called a Safety Data Sheet or SDS/MSDS for short because it's being sent internationally and has a battery included in the box.
I called Apple and spoke to a specialist who told me they can only access it if the product is shipped to home and not picked up in store but every sds is he same , so you've guessed it, could someone take 5 minutes out of their day and request this who had it delivered? I guess it's just a pdf but it might be helpful for a few others too.
Thankyou so much in advance and hope you're enjoying your Vision Pro.

We bought some used rain barrels today that were sold as "food grade." One conyained propylene glycol excipient (food use only); the other, polyethylene glycol 400 NF (it's label says "not a dangerous substance or mixture according to GHS).
Question: I read the MSDS sheets for both, and it appears neither poses a hazard. But I am just a regular guy, and wanted the experts to chime in. What say you, please? Can these barrels be safgely used to catch rain from our roof spouts and then use in our garden?
​

Brand new seller here… I am evaluating a product that is powered by small polymer lithium ion battery built in. I am creating a listing to see if Amazon would let me sell this item (by submitting an exemption sheet). But then I looked competitors who sell the same product… their listing didn’t even show battery information or it is a dangerous good/hazmat. I am so confused… did they knowingly list a product in the wrong category or omit detail about battery?
I want to do it the right way. My research leads me to submitting an exemption sheet because the product itself does not have a MSDS; rather only the lithium polymer battery has a MSDS. Any guidance is appreciated! Cheers everyone!