Label: EQUATE- ethyl alcohol gel

  • NDC Code(s): 79903-144-03, 79903-144-12, 79903-144-32, 79903-144-60
  • Packager: Wal-Mart Stores Inc.
  • 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 November 13, 2022

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  • ACTIVE INGREDIENT

    Ethyl Alcohol 70%

  • PURPOSE

    Antiseptic

  • 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.

    ■ 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 a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    ■ 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.

  • INDICATIONS & USAGE

    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.

  • STORAGE AND HANDLING

    ■ Store at a temperature below 110ºF (43ºC) ■ Avoid freezing and excessive heat above 104°F (40°C)

  • INACTIVE INGREDIENT

    Water (Aqua), PEG-6, AMP-Acrylates/Vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Isopropyl Alcohol, Glycerin,
    Isopropyl Myristate, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Yellow 5 (Cl 19140), Blue 1 (Cl 42090).

  • PRINCIPAL DISPLAY PANEL

    60 oz 32 oz12 oz3 oz

  • INGREDIENTS AND APPEARANCE
    EQUATE 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-144
    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
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    PEG-6 ISOSTEARATE (UNII: 0E2639OTJY)  
    HC YELLOW NO. 5 (UNII: I844A312T7)  
    DIRECT BLUE 1 (UNII: 8NN34MAQ6H)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-144-0389 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2022
    2NDC:79903-144-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2022
    3NDC:79903-144-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2022
    4NDC:79903-144-601770 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/13/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/13/2022
    Labeler - Wal-Mart Stores Inc. (051957769)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(79903-144)
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