Label: CL LIGHT- garcinia gummi-gutta fruit, caffeine cream

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated August 30, 2018

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Garcinia Cambogia Fruit Extract, Caffeine

  • INACTIVE INGREDIENT

    Jania Rubens Extract, Laminaria Digitata Extract, Water, etc.

  • PURPOSE

    Giving aid to reduce temporary cellulite

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children


  • WARNINGS

    Consult a physician if you have any abnormal symptoms such as red spots, swelling or itching, or side effects caused by direct sunlight.

  • DOSAGE & ADMINISTRATION

    for external use only


  • INDICATIONS & USAGE

    Apply it as a massge befor exercie, after shower.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CL LIGHT 
    garcinia gummi-gutta fruit, caffeine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70042-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE0.63 g  in 100 mL
    GARCINIA GUMMI-GUTTA FRUIT (UNII: D0QJI8UQVR) (GARCINIA GUMMI-GUTTA FRUIT - UNII:D0QJI8UQVR) GARCINIA GUMMI-GUTTA FRUIT0.04 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70042-0003-12 mL in 1 POUCH; Type 0: Not a Combination Product08/30/2018
    2NDC:70042-0003-3500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/30/2018
    3NDC:70042-0003-2200 mL in 1 TUBE; Type 0: Not a Combination Product08/30/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/30/2018
    Labeler - Powerful X (689515038)
    Registrant - Powerful X (689515038)
    Establishment
    NameAddressID/FEIBusiness Operations
    Powerful X689515038manufacture(70042-0003) , label(70042-0003) , pack(70042-0003)