Label: ALCOHOL ANTISEPTIC PADS- isopropyl alcohol swab

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

Drug Label Information

Updated March 11, 2026

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  • Active Ingredients

    Isopropyl alcohol 70% v/v

  • Purpose

    Antiseptic Cleanser

  • Use

    For preparation of the skin prior to injection

  • Warnings

    For external use only. Flammable; keep away from fire or flame.

  • OTC - KEEP OUT OF REACH OF CHILDREN SECTION

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Do not use

    with electrocautery procedures, in the eyes, if contact occurs, flush eyes with water.

  • Stop Use

    if irritation or redness develop. If condition persists consult your health care practitioner.

  • Directions

    Wipe injection site vigorously and discard.

  • Other information

    Sterile unless pouch is opened or damaged. Store at room temperature 15º - 30º C ( 59º - 86º F)

  • Inactive Ingredient Section

    Purified Water

  • Questions

    800.835.2263

  • Principal Display Panel

    Carton Image

  • INGREDIENTS AND APPEARANCE
    ALCOHOL ANTISEPTIC PADS 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0020(NDC:60913-047)
    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:0924-0020-0210 in 1 CARTON03/30/2026
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:0924-0020-0420 in 1 CARTON03/30/2026
    21 mL in 1 PACKET; Type 0: Not a Combination Product
    3NDC:0924-0020-0550 in 1 CARTON03/30/2026
    31 mL in 1 PACKET; Type 0: Not a Combination Product
    4NDC:0924-0020-07100 in 1 CARTON03/30/2026
    41 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/30/2026
    Labeler - Acme United Corporation (001180207)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation045924339repack(0924-0020) , relabel(0924-0020)
    Establishment
    NameAddressID/FEIBusiness Operations
    Acme United Corporation080119599repack(0924-0020) , relabel(0924-0020)
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