Label: ALCOHOL gel

  • NDC Code(s): 82442-002-02, 82442-002-08, 82442-002-32
  • Packager: TARGET CORPORATION INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 10, 2024

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  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    For personal hand hygine 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.

    Do not use

    • On infants less than 2 months of age.
    • On open skin wounds
    • On broken or damaged skin.

    When using this product

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

    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 Poison Control Center immediately.

  • Directions

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

    • Store between 15 - 30 o C (59-86 oF).
    • Avoid Freezing and excessive heat above 40 oC (104 oF)
  • Inactive Ingredients

    Water (Aqua), PEG-6, AMP-Acrylates/vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Isopropyl Alcohol, Glycerin,Isopropyl Myristate, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.

  • Questions

    1-800-910-6874

  • Package 2 FL Oz

    Principal Display Panel

  • Package 8 FL Oz

    Principal Display Panel

  • Package 32 FL Oz

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-002-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2024
    2NDC:82442-002-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2024
    3NDC:82442-002-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/01/2024
    Labeler - TARGET CORPORATION INC. (006961700)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(82442-002)
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