CAFFÉ MACCHIATO DECAF (8SACHETS/POUCH)
DECAF CAFFÉ MACCHIATO 8 SACHETS/POUCH INSTANT MIX COLLAGEN CANDIDATE REDUCED GLUTATHIONE CANDIDATE L-CARNITINE CANDIDATE CHITOSAN CANDIDATE INULIN FIBER CANDIDATE DAILY USE TRAVEL-FRIENDLY LUXE SLIM.
BEVERAGEINSTANT COFFEEDECAFFEINATED SLIMMING DRINK

CAFFÉ MACCHIATO DECAF (8SACHETS/POUCH)

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₱355.00

A premium beauty product from LUXE SLIM.

Brand: LUXE SLIM

Category: BEVERAGE,INSTANT COFFEE,DECAFFEINATED SLIMMING DRINK

Stock: CAFFÉ MACCHIATO DECAF 8'S POUCH available

Tags: DECAF, CAFFÉ MACCHIATO, 8 SACHETS/POUCH, INSTANT MIX, COLLAGEN CANDIDATE, REDUCED GLUTATHIONE CANDIDATE, L-CARNITINE CANDIDATE, CHITOSAN CANDIDATE, INULIN FIBER CANDIDATE, DAILY USE, TRAVEL-FRIENDLY, LUXE SLIM.

FDA Information

Certificate 1

Expiration: June 5, 2029
CAFFE MACCHIATO DECAF POWDERED DRINK MIX WITH COLLAGEN, GLUTATHIONE, CHITOSAN, INULIN FIBER, L-CARNITINE PACKED IN PLASTIC SACHET AND PLASTIE JAR MAGKAWAS BEAUTY AND WELLNESS OPC, DIZON COMPOUND, G. MARCELO COR., O. MIRANDA ST. MAYSAN, VALENZUELA CITY, METRO MANILA CFRR-NCR-FT-453025 FDA REGISTRATION NO .: FR-4000013033666 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, RALES AND REGULATIONS, THE REGISTRATION OF THE HIGH RISK FOOD PRODUCT DESCRIBED HEREUNDER IS GRANTED APPROVAL. BRAND NAME: LUXE SLIM PRODUET NAME: PACKAGING: COMPANY NAME AND ADDRESS: LTO NO .: 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 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 05 JUNE 2024 AND VALID UNTIL 05 JUNE 2029.
FDA Document