Label: WRINKLE POWER FILLING- glycerin gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 13, 2020

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  • ACTIVE INGREDIENT

    Glycerin

  • INACTIVE INGREDIENT

    Water, Propylene Glycol, Biotin, Aloe Barbadensis Leaf Extract, Adenosine, Allantoin, etc.

  • PURPOSE

    Skin protectant - Wrinkle Care

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    [How to Use]

    1. Towel dry after face washing.
    2. Apply thin layer to the direction of wrinkle. Keep patting gently for about 15 seconds.
    3. Try not to talk or move for at least 2 minutes until dry.
    4. Strain feeling of your skin will disappear naturally.
    • Shake well before you use.
    • The nature of Hydrolyzed Sponge, it may be pricking little bit depends on individual's skin condition. However, it is quite natural and proving for working to your skin.
  • WARNINGS

    [Caution]

    1. Use only directed.
    2. Avoid stroing in extremely high or low temperatures and areas exposed to direct sunlight.
    3. If irritation occurs, discontinue use.
  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    WRINKLE POWER FILLING 
    glycerin gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72176-0100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3.55 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ADENOSINE (UNII: K72T3FS567)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72176-0100-16 mL in 1 SYRINGE, PLASTIC; Type 0: Not a Combination Product03/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34703/01/2018
    Labeler - GIBEST (689837540)
    Registrant - GIBEST (689837540)
    Establishment
    NameAddressID/FEIBusiness Operations
    GIBEST689837540manufacture(72176-0100)
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