CAFFÉ TURMERICO JAR 500GRAMS
TURMERIC COFFEE 500G JAR HYDROLYZED MARINE COLLAGEN REDUCED L-GLUTATHIONE PHARMA GABA IMMUNITY SUPPORT ANTI-INFLAMMATORY NON-ACIDIC KETO-FRIENDLY DIABETIC-FRIENDLY LUXE SLIM
BEVERAGEINSTANT COFFEEFUNCTIONAL DRINK

CAFFÉ TURMERICO JAR 500GRAMS

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₱965.00

A premium beauty product from LUXE SLIM.

Brand: LUXE SLIM

Category: BEVERAGE,INSTANT COFFEE,FUNCTIONAL DRINK

Stock: CAFFÉ TURMRCO JAR available

Tags: TURMERIC COFFEE, 500G JAR, HYDROLYZED MARINE COLLAGEN, REDUCED L-GLUTATHIONE, PHARMA GABA, IMMUNITY SUPPORT, ANTI-INFLAMMATORY, NON-ACIDIC, KETO-FRIENDLY, DIABETIC-FRIENDLY, LUXE SLIM

FDA Information

Certificate 1

Expiration: September 12, 2029
PRODUCT NAME: PACKAGING: COMPANY NAME AND ADDRESS: LTO NO .: FDA REGISTRATION NO .: FR-4000013013390 CERTIFICATE OF PRODUCT REGISTRATION (HIGH RISK FOOD PRODUET) 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 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: LUXE SLIM CAFFE TURMERICO COFFEE POWDERED DRINK MIX WITH TURMERIC, REDUCED L-GLUTATHIONE, HYDROLYZED MARINE COLLAGEN PACKED IN PLASTIC SACHET AND PLASTIC JAR MAGKAWAS BEAUTY AND WELLNESS OPC, DIZON COMPOUND, G. MARCELO COR., O. MIRANDA ST. MAYSAN, VALENZUELA CITY, METRO MANILA CFRR-NCR-FT-453025 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 PEODUCT 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 PRODUET BE COMMITTED. ISSUED ON 12 SEPTEMBER 2024 AND VALID UNTIL 12 SEPTEMBER 2029.
FDA Document