DIAMOND BRIGHT SHEET MASK (5PCS/BOX)
104 sold DIAMOND BRIGHT BRIGHTENING HYDRATING FIRMING REVITALIZING 30 ML PER SHEET 5 PCS PER PACK INSTANT GLOW EVEN SKIN TONE PLANT-BASED SUSTAINABLY SOURCED WEEKLY TREATMENT BYFINA BEAUTY
SKINCAREBRIGHTENING SHEET MASKFACIAL TREATMENT

DIAMOND BRIGHT SHEET MASK (5PCS/BOX)

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₱459.00

A premium beauty product from BYFINA BEAUTY.

Brand: BYFINA BEAUTY

Category: SKINCARE, BRIGHTENING SHEET MASK, FACIAL TREATMENT

Stock: BYFINA SHEET MASK available

Tags: DIAMOND BRIGHT, BRIGHTENING, HYDRATING, FIRMING, REVITALIZING, 30 ML PER SHEET, 5 PCS PER PACK, INSTANT GLOW, EVEN SKIN TONE, PLANT-BASED, SUSTAINABLY SOURCED, WEEKLY TREATMENT, BYFINA BEAUTY

FDA Information

Certificate 1

Expiration: June 9, 2026 (Expired)
NN-1000014747727 09 JUNE 2026 BYFINA BYFINA DIAMOND BRIGHT BRIGHTENING MASK N.A. GUANGZHOU JIUGONGYANHUA BIOTECHNOLOGY CO., LTD NO. 3 YIHENG ROAD, QINGHU MATIAN STREET, JUNHE STREET, BIAYUN DISTRICT, GUANGZHOU CITY, GUANGDON PROVINCE CHINA NAME OF THE COMPANY: ADDRESS OF THE COMPANY: LTO NUMBER: NOTIFICATION OF COSMETIC PRODUCT PURSUANT TO THE EXISTING RULES AND REGULATIONS OF THE FOOD AND DRUG ADMINISTRATION (FDA) FOR THE NOTIFICATION OF COSMETIES, THE PRODUCT NOTIFICATION IS HEREBY ACKNOWLEDGED, COSMETIC NOTIFICATION NUMBER: VALIDITY: PARTICULARS OF THE PRODUCT BRAND NAME: PRODUCT NAME: VARIANT/S: PARTICULARS OF THE MANUFACTURER NAME OF THE MANUFACTURER: ADDRESS OF THE MANUFACTURER: COUNTRY OF MANUFACTURE: PARTICULARS OF THE LOCAL COMPANY RESPONSIBLE FOR PLACING THE PRODUCT IN THE MARKET STREAM NATION PH, INC. UNIT E G/F 9673 PILILIA COR. OBRERO STS., VALENZUELA, MAKATI, METRO MANILA LTO-3000014279677 THE PRODUCT IS ALLOWED TO BE SOLD IN THE LOCAL MARKET SUBJECT TO COMPLIANCE WITH THE REQUIREMENTS OF THE ASEAN COSMETIC DIRECTIVE AND THE FDA LAWS, AND ITS IMPLEMENTING RULES AND REGULATIONS. THIS NOTIFICATION SHOULD NOT BE TAKEN AS A GUARANTEE AND/OR ENDORSEMENT OF THE SAFETY, QUALITY, AND CLAIMED BENEFIT OF THE PRODUCT. ANY SUBSEQUENT CHANGES TO THE INFORMATION SUBMITTED IN THIS NOTIFICATION WILL RENDER THIS NOTIFICATION INVALID AND A NEW NOTIFICATION WILL HAVE TO BE SUBMITTED. 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 CONSIGNMENT OF THE PRODUCT CONTINUES TO MEET ALL THE LEGAL REQUIREMENTS, AND CONFORMS TO ALL THE STANDARDS AND SPECIFICATIONS OF THE PRODUCT DECLARED TO THE FDA. THIS 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.
FDA Document