Skin lightening and whitening
My product is flagged as skin whitening.
Can anyone advise on the following:
1) Will a Mercury test result from a labs outside USA be sufficient or it must comes from a domestic lab?
2) The FDA is no longer accepting submissions for FDA's Voluntary Cosmetic Registration Program (VCRP) - Form FDA 2511 (21 CFR Part 710) and Form FDA 2512 (21 CFR Part 720), as they prepare for the new regulation coming into placed called MOCRA. Why is Amazon still asking for these forms?
3) Also, does the name of the manufacturer must match the listing's manufacturer? These FDA forms would come from my supplier but I list myself as the product's manufacturer (as the matter of fact we don't disclose our supplier on the listing)
Thanks
Skin lightening and whitening
My product is flagged as skin whitening.
Can anyone advise on the following:
1) Will a Mercury test result from a labs outside USA be sufficient or it must comes from a domestic lab?
2) The FDA is no longer accepting submissions for FDA's Voluntary Cosmetic Registration Program (VCRP) - Form FDA 2511 (21 CFR Part 710) and Form FDA 2512 (21 CFR Part 720), as they prepare for the new regulation coming into placed called MOCRA. Why is Amazon still asking for these forms?
3) Also, does the name of the manufacturer must match the listing's manufacturer? These FDA forms would come from my supplier but I list myself as the product's manufacturer (as the matter of fact we don't disclose our supplier on the listing)
Thanks
0 replies
Manny_Amazon
Hello @Seller_KhXhSXj4BUx8c,
Thanks for posting to the Forums. You will find more detail about this policy in the Skin lightening and whitening products page. To answer your questions:
- As long as you use the regulation/standard requirements listed, whether domestically or internationally, that should be sufficient.
- Amazon will be asking for those forms as long as the requirement exists. Amazon will update to the new regulation once it is fully deployed by the FDA. If you have any questions, you can create a case with the Compliance team and ask those questions (you'll find it under "how to submit information" in the above help page). You can use the service provider network for help with the testing documents.
- This must be documentation that demonstrates participation by the selling partner, manufacturer, packer, or distributor of the product in the FDA’s Voluntary Cosmetic Registration Program (VCRP) – Form FDA 2511 (must match the product manufacturer listed on the product)
I hope this information helps.
- Manny
