HEERA GLOW 20 IN 1 (60 CAPSULES)

PRODUCT NAME: PACKAGING: FDA REGISTRATION NO .: FR-4000013253664 CERTIFICATE OF PRODUCT REGISTRATION 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: HEERA GLOW 20IN1 COLLAGEN + GLUTATHIONE + ROSEHIPS + CENTELLA ASIATICA FOOD SUPPLEMENT CAPSULE (REGISTERED AS FOOD SUPPLEMENT WITH NO APPROVED THERAPEUTIC CLAIMS) WHITE CAPSULE SHAPED PLASTIC BOTTLE BY 60`S 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 OCTOBER 2024 AND VALID UNTIL 17 OCTOBER 2026.