Label: G3S AMPOULE- glycerin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 March 22, 2017

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  • ACTIVE INGREDIENT

    Active ingredients: GLYCERIN 1.0%

  • INACTIVE INGREDIENT

    Inactive ingredients: Aqua (Water), Propylene Glycol, Glycoproteins, Glutamic Acid, Glycine Soja PROTEIN, Ceratonia Siliqua GUM, Phenoxyethanol, Disodium Cocoamphodiacetate, Sodium Dextran Sulfate, Valine, Glycine, Threonine, Sodium Benzoate, Potassium Sorbate, Triethanolamine, Carbomer, Gold 23 k

  • PURPOSE

    Purpose: Skin moisturizing and lifting

  • WARNINGS

    Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS & USAGE

    Indications & Usage: Apply morning and night

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: Apply morning and night to the entire face and neck prior to moisturizers or facial masks

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    G3S AMPOULE 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71276-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.02 g  in 2 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71276-110-0210 in 1 CARTON03/02/2017
    1NDC:71276-110-012 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/02/2017
    Labeler - ULAB (688976692)
    Registrant - ULAB (688976692)
    Establishment
    NameAddressID/FEIBusiness Operations
    ULAB688976692relabel(71276-110)
    Establishment
    NameAddressID/FEIBusiness Operations
    U-LAB Switzerland AG485958743manufacture(71276-110)