On September 9, 2026, the U.S. Food and Drug Administration clarified an important point for cosmetic companies and retailers: FDA does not issue certificates or verification letters for cosmetic facility registration or product listing. A registration or listing number also does not mean that FDA has approved a facility or product. For a US hair color brand choosing an OEM hair color manufacturer, this changes the right first question from “Can you show an FDA certificate?” to “Can you support the records and responsibilities behind a compliant market launch?”
Under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA), manufacturers and processors generally must register covered cosmetic facilities and renew those registrations every two years. The responsible person—normally the manufacturer, packer, or distributor named on the label—must list each marketed cosmetic product with its ingredients and update the listing annually.
These submissions matter, but the FDA says they are not an approval program or a promotional tool. Buyers should therefore avoid treating a number, screenshot, badge, or seller-created certificate as complete proof of compliance.
Before approving samples or packaging, brands, distributors, and salon-supply sellers should align with their hair dye factory on five practical items:
Hair color needs additional label attention. FDA guidance explains that coal-tar hair dyes have specific statutory caution and preliminary skin-test directions, while other color additives must meet applicable approval, use, and labeling requirements. The exact pathway depends on the product and ingredients, so it should be confirmed before artwork is finalized.
A professional private label hair color supplier should start with the target market, product category, intended professional use, shade plan, formula direction, pack size, artwork language, and expected order volume. Famo Kemei Innovation (Guangdong) Cosmetics Co., Ltd. supports OEM, ODM, and OBM discussions for hair color, perm, bleaching, and hair-care products. Compliance documents, responsibilities, and claims are confirmed for each project rather than assumed from a generic badge.
For US-bound sourcing, ask for a project review that connects formula, label, packaging, batch records, and post-market responsibilities before commercial production. Explore our hair color cream range or contact our team with your market and product brief.
Company: Famo Kemei Innovation (Guangdong) Cosmetics Co., Ltd.
Contact: Ted, Founder & CEO
Phone / WhatsApp / WeChat: +86 183 4438 3713
Address: 2nd to 3rd Floor, Building D5-3, East of Gongye Avenue, South of Hengsi Road, Zhongqu, Qinghuayuan, Donghua Town, Yingde City, Qingyuan City, Guangdong Province, China
On September 9, 2026, the U.S. Food and Drug Administration clarified an important point for cosmetic companies and retailers: FDA does not issue certificates or verification letters for cosmetic facility registration or product listing. A registration or listing number also does not mean that FDA has approved a facility or product. For a US hair color brand choosing an OEM hair color manufacturer, this changes the right first question from “Can you show an FDA certificate?” to “Can you support the records and responsibilities behind a compliant market launch?”
Under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA), manufacturers and processors generally must register covered cosmetic facilities and renew those registrations every two years. The responsible person—normally the manufacturer, packer, or distributor named on the label—must list each marketed cosmetic product with its ingredients and update the listing annually.
These submissions matter, but the FDA says they are not an approval program or a promotional tool. Buyers should therefore avoid treating a number, screenshot, badge, or seller-created certificate as complete proof of compliance.
Before approving samples or packaging, brands, distributors, and salon-supply sellers should align with their hair dye factory on five practical items:
Hair color needs additional label attention. FDA guidance explains that coal-tar hair dyes have specific statutory caution and preliminary skin-test directions, while other color additives must meet applicable approval, use, and labeling requirements. The exact pathway depends on the product and ingredients, so it should be confirmed before artwork is finalized.
A professional private label hair color supplier should start with the target market, product category, intended professional use, shade plan, formula direction, pack size, artwork language, and expected order volume. Famo Kemei Innovation (Guangdong) Cosmetics Co., Ltd. supports OEM, ODM, and OBM discussions for hair color, perm, bleaching, and hair-care products. Compliance documents, responsibilities, and claims are confirmed for each project rather than assumed from a generic badge.
For US-bound sourcing, ask for a project review that connects formula, label, packaging, batch records, and post-market responsibilities before commercial production. Explore our hair color cream range or contact our team with your market and product brief.
Company: Famo Kemei Innovation (Guangdong) Cosmetics Co., Ltd.
Contact: Ted, Founder & CEO
Phone / WhatsApp / WeChat: +86 183 4438 3713
Address: 2nd to 3rd Floor, Building D5-3, East of Gongye Avenue, South of Hengsi Road, Zhongqu, Qinghuayuan, Donghua Town, Yingde City, Qingyuan City, Guangdong Province, China