SUN BOUNCE DAILY TINTED SUNSCREEN TUBE

COSMETIC NOTIFICATION NUMBER: VALIDITY: PARTICULARS OF THE PRODUCT BRAND NAME: PRODUCT NAME: VARIANT/S: NOTIFICATION OF COSMETIC PRODUCT PURSUANT TO THE EXISTING RULES AND REGULATIONS OF THE FOOD AND DRUG ADMINISTRATION (FDA) FOR THE NOTIFICATION OF COSMETICS, THE PRODUCT NOTIFICATION IS HEREBY ACKNOWLEDGED, NN-1000015017812 24 JULY 2026 DEAR FACE SUNBOUNCE DAILY TINTED SUNSCREEN SUNBOUNCE DAILY TINTED SUNSCREEN 30ML (SOLO), SUNBOUNCE DAILY TINTED SUNSCREEN 30ML+30ML (TWIN), SUNBOUNCE DAILY TINTED SUNSCREEN 50ML (TUBE) NAME OF THE COMPANY: ADDRESS OF THE COMPANY: LTO NUMBER: PARTICULARS OF THE LOCAL COMPANY RESPONSIBLE FOR PLACING THE PRODUCT IN THE MARKET ISAIAH888 BEAUTY INNOVATIONS INC. DOING BUSINESS UNDER THE NAME AND STYLE OF DEAR FACE ANDALUCIA ST., DULONG BAYAN , BACOOR, CAVITE 3000012216696 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.