Label: WINTER FROST HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 63148-727-02
  • Packager: Apollo Health and Beauty Care
  • 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 July 15, 2021

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  • Active Ingredients

    Ethyl Alcohol (70%)

  • Purpose

    Antiseptic

  • Uses

    For Personal hand hygiene to help prevent the spread of bacteria and can be used in place of hand washing if soap and water are not available.

  • Warnings

    • For External use only
    • Flammable
    • Keep away from source of heat or fire. 

    When using this product

    Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not Inhale.

    Do not use

    • on children less than 2 months of age
    • on open skin wounds
    • on broken or damaged skin

    Stop use and ask a doctor

    If Irritation or redness develops and lasts.

    Keep out of reach of children

    In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately

  • Directions

    • For occasional and personal use
    • Rub thoroughly into hands for at least 30 seconds. Allow to dry
    • Children under 6 years should be supervised when using this product
  • Other Information

    • Store at a temperature below 1100F (430C)
    • May discolor certain fabrics or surfaces
  • Inactive Ingredients

    Water (Aqua), PEG-6, AMP-Acrylates/Vinyl Isodecanate Crosspolymer, Fragrance (Parfum), Isopropyl Myristate, Glycerin, Isopropyl Alcohol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Blue 1 (Cl42090)

  • Principal Display Panel

    Winter Frost-01Winter Frost-02

  • INGREDIENTS AND APPEARANCE
    WINTER FROST HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-727
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIRECT BLUE 1 (UNII: 8NN34MAQ6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63148-727-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/08/2021
    Labeler - Apollo Health and Beauty Care (201901209)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(63148-727)
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