Label: ALCOHOL PREP- isopropyl alcohol swab

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

Drug Label Information

Updated December 27, 2023

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  • Active ingredient

    Isopropyl Alcohol, 70% v/v

  • Purpose

    Antiseptic

  • Uses

    • First aid to decrease germs in minor cuts, scrapes and burns.
  • Warnings

    • For external use only.
    • Flammable. Keep away from fire or flame.

    Do not use

    • with electrocautery procedures
    • longer than 1 week unless directed by a doctor

    When using this product

    • do not get into eyes
    • do not apply over large areas of the body
    • in case of deep or puncture wounds, animal bites or serious burns, consult a doctor

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition gets worse or persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    • Apply to skin as needed
    • Discard after single use
  • Other information

    Protect from freezing and avoid excessive heat.

  • Inactive ingredients

    water

  • Manufacturing Information

    Distributed By:

    Topco Associates LLC.

    Elk Grove Village, IL 60007

    ©TopCo MDLA0618

    Questions? 1-888-423-0139

    topcare@topco.com

    www.topcarebrand.com

    Made in China

    RD20LPD

  • Principal Display Panel

    Package Label

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76162-809
    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:76162-809-30100 in 1 BOX07/13/201112/31/2026
    11 in 1 PACKET
    10.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/13/201112/31/2026
    Labeler - Topco Associates (006935977)
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