Label: ALCOHOL WIPE- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 17, 2024

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  • ACTIVE INGREDIENT

    Isopropyl Alcohol 70%

  • PURPOSE

    First aid Antiseptic

  • INDICATIONS & USAGE

    First aid to help prevent the risk of infection in minor cuts, scrapes or burns.

  • WARNINGS

    For external use only

  • SAFE HANDLING WARNING

    Flammable keep away from fire or flame

  • ASK DOCTOR

    Deep or puncture wounds

    animal bites

    serious burns

  • WHEN USING

    Do not use in or near the eyes

    Do not apply over large areas

    Do not use longer than 1 week unless directed by doctor

  • STOP USE

    Stop use and ask doctor if condition persists or get worse

  • If swallowed, get medical help or contact a Poison control center right away

  • DOSAGE & ADMINISTRATION

    Clean the affected area

    Apply product on the affected area of the body 1 to 3 times a day

    The affected area could be covered with a sterile bandage

  • OTHER SAFETY INFORMATION

    For external use only

    Keep the canister tightly closedand store it at room temperature

    Hold it away from face when opening

  • INACTIVE INGREDIENT

    Purified water

  • QUESTIONS

    18002102060

  • PRINCIPAL DISPLAY PANEL

    Equate Alcohol Wipes

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPE 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-227
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-227-4040 in 1 CANISTER09/29/2023
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/29/2023
    Labeler - Walmart Inc. (051957769)
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