Label: BIELLEE POLLEN WHITENING WRINKLE TIME REPAIR AMPOULE- glycerin cream

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

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Drug Label Information

Updated June 21, 2016

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  • ACTIVE INGREDIENT

    GLYCERIN 12.00%

  • PURPOSE

    Skin Protectant

  • INDICATIONS & USAGE

    Temporarily protects chapped or cracked skin
    Prevent and protect from the drying effects of wind and cold weather

  • DOSAGE & ADMINISTRATION

    Apply liberally as needed onto clean facial skin day or night
    Children under 6 months: ask a doctor

  • WARNINGS

    For external use only

    Do not use on damaged or broken skin

    When using this product, keep out of eyes. Rinse with water to remove.

    Stop using and ask a doctor if rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

  • INACTIVE INGREDIENT

    WATER
    POLLEN EXTRACT
    DIPROPYLENE GLYCOL
    BUTYLENE GLYCOL
    MORINDA CITRIFOLIA FRUIT EXTRACT
    ALCOHOL
    NIACINAMIDE
    PHENOXYETHANOL
    FRAGRANCE
    PEG-40 HYDROGENATED CASTOR OIL
    PPG-26-BUTETH-26
    CARBOMER
    XANTHAN GUM
    ALLANTOIN
    SODIUM HYALURONATE
    POTASSIUM HYDROXIDE
    ETHYLHEXYLGLYCERIN
    DISODIUM EDTA

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    BIELLEE POLLEN WHITENING WRINKLE TIME REPAIR AMPOULE 
    glycerin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70784-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN1.2 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BEE POLLEN (UNII: 3729L8MA2C)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    NONI FRUIT (UNII: 7829X3G2X5)  
    ALCOHOL (UNII: 3K9958V90M)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ALLANTOIN (UNII: 344S277G0Z)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70784-001-023 in 1 CARTON06/21/2016
    1NDC:70784-001-0110 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/21/2016
    Labeler - NSB CO., LTD. (689846922)
    Registrant - NSB CO., LTD. (689846922)
    Establishment
    NameAddressID/FEIBusiness Operations
    NSB CO., LTD.689846922manufacture(70784-001)
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