HOPE GLOW SUPER BIGGIE (60CAPS/POUCH)

GLUTATHIONE + ALPHA LIPOIC ACID + SODIUM ASCORBATE FOOD SUPPLEMENT CAPSULES (REGISTERED AS FOOD SUPPLEMENT WITH NO APPROVED THERAPEUTIC CLAIMS) POUCH OF 14 AND 60 MYHOPE BEAUTY AND WELLNESS PRODUCTS TRADINC, - CFRR-NCR-FT-723786 FDA REGISTRATION NO .: FR-4000013472366 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 REPUBLIE 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 PRODUET DESCRIBED HEREUNDER IS GRANTED APPROVAL. BRAND NAME: LUNA AURA HOPE GLOW SUPER PRODUCT NAME: 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 17 DECEMBER 2024 AND VALID UNTIL 17 DECEMBER 2026.