BEAUTY MILK MELON 18G (1SACHET)
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Beauty Product

BEAUTY MILK MELON 18G (1SACHET)

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Brand: DEAR FACE - BEAUTY MILK
Product Name: BEAUTY MILK MELON 18G (1SACHET)

Brand: DEAR FACE - BEAUTY MILK

Category: N/A

Stock: BM MELON (1SACHET) available

FDA Information

Certificate 1

Expiration: November 20, 2026
PACKAGING: COMPANY NAME AND ADDRESS: LTO NO .: MANUFACTURER NAME AND ADDRESS: THE COMPANY HEREBY ENSURES THAT THEY SHALL RESPOND AND COOPERATE FULLY WITH THE FDA WITH REGARD TO ANY SUBSEQUENT POST-MARKETING ACTIVITY INITIATED BY THE FDA. FURTHER, THE COMPANY SHALL BE RESPONSIBLE FOR ENSURING THAT EACH BATCH/LOT OF THE PRODUCT CONTINUES TO MEET ALL THE LEGAL REQUIREMENTS, AND CONFORMS TO ALL THE STANDARDS AND SPECIFICATION OF THE PRODUCT DECLARED TO THE FDA, INCLUDING COMPLIANCE TO THE LIST OF OBLIGATIONS ENUMERATED AT THE REVERSE SIDE OF THIS DOCUMENT. THE AUTHORIZATION IS SUBJECT TO SUSPENSION, CANCELLATION, OR RECALL SHOULD ANY VIOLATION OF FDA LAWS, AND ITS IMPLEMENTING RULES AND REGULATIONS, INVOLVING THE PRODUCT BE COMMITTED. ISSUED ON 20 NOVEMBER 2024 AND VALID UNTIL 20 NOVEMBER 2026. BY AUTHORITY OF THE DIRECTOR GENERAL FDA REGISTRATION NO .: FR-4000013249863 CERTIFICATE OF PRODUCT REGISTRATION (HIGH RISK FOOD PRODUCT) PURSUANT TO THE PROVISIONS OF REPUBLIC ACT NO.3720, OTHERWISE KNOWN AS THE FOOD, DRUGS AND DEVICES, AND COSMETIC ACT, AS AMENDED BY EXECUTIVE ORDER NO. 175, AND REPUBLIC ACT NO. 9711, OTHERWISE KNOWN AS THE FOOD AND DRUG ADMINISTRATION ACT OF 2009, AND OTHER APPLICABLE LAWS, RULES AND REGULATIONS, THE REGISTRATION OF THE HIGH RISK FOOD PRODUCT DESCRIBED HEREUNDER IS GRANTED APPROVAL. BRAND NAME: DEAR FACE BEAUTY MILK PRODUCT NAME: JAPANESE STYLE COLLAGEN FOOD SUPPLEMENT POWDER-MELON FLAVOR (REGISTERED AS FOOD SUPPLEMENT WITH NO APPROVED THERAPEUTIC CLAIMS) 18 GRAMS X 10 SACHETS ISAIAH888 BEAUTY INNOVATIONS INC. DOING BUSINESS UNDER THE NAME AND STYLE OF DEAR FACE, ANDALUCIA ST. DULONG BAYAN, BACOOR CITY, CAVITE CFRR-RIVA-FT-911762 PILAR MARILYN M. PAGAYUNAN DIRECTOR IV, CENTER FOR FOOD REGULATION AND RESEARCH
FDA Document