STRAWBERRY CREAM 180G (10SACHETS/POUCH)
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Beauty Product

STRAWBERRY CREAM 180G (10SACHETS/POUCH)

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₱429.00

A premium beauty product from DEAR FACE - BEAUTY MILK.

Brand: DEAR FACE - BEAUTY MILK

Category: N/A

Stock: BM STRWBRRY CREAM available

FDA Information

Certificate 1

Expiration: November 20, 2026
PRODUCT NAME: PACKAGING: COMPANY NAME AND ADDRESS: LTO NO .: FDA REGISTRATION NO .: FR-4000014110470 CERTIFICATE OF PRODUCT REGISTRATION (HIGH RISK FOOD PRODUCT) PURSUANT TO THE PROVISIONS OF REPUBLIC ACT NO.3720, OTHERWISE KNOWN AS THE FOOD, DRAGS 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 STRAWBERRIES & CREAM WITH ASHWAGANDHA + GLUTATHIONE + COLLAGEN POWDERED DRINK MIX 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 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 PRODUET 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 16 APRIL 2025 AND VALID UNTIL 16 APRIL 2027. BY AUTHORITY OF THE DIRECTOR GENERAL DR. SAMUEL A. ZACATE MAKRPKFAGAL PILAR MARILYN M. PAGAYUNAN DIRECTOR IV, CENTER FOR FOOD REGULATION AND RESEARCH
FDA Document