HOPE GLOW LIGHT

PRODUCT NAME: PACKAGING: COMPANY NAME AND ADDRESS: LTO NO .: FDA REGISTRATION NO .: FR-4000014933462 CERTIFICATE OF PRODUCT REGISTRATION (HIGH RISK FOOD PRODUCT) PURSUANT TO THE PROVISIONS OF REPUBLIE 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 PRODUCT DESCRIBED HEREUNDER IS GRANTED APPROVAL. BRAND NAME: LUNA AURA HOPE GLOW LIGHT GARCINIA CAMBOGIA, L-CARNITINE, GREEN TEA, DANDELION AND COLLAGEN FOOD SUPPLEMENT CAPSULE (REGISTERED AS FOOD SUPPLEMENT WITH NO APPROVED THERAPEUTIC CLAIMS) 500 MG (30 CAPSULES) MYHOPE BEAUTY AND WELLNESS PRODUCTS TRADING, 99 BALETE DRIVE EXTENSION KRISTONG HARI, QUEZON CITY, METRO MANILA CFRR-NCR-FT-723786 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, INELUDING 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 14 AUGUST 2025 AND VALID UNTIL 14 AUGUST 2027.