Label: ALCOHOL PREP PADS- isopropyl alcohol swab

  • NDC Code(s): 67510-0251-2, 67510-0251-4, 67510-0251-5
  • Packager: Kareway Product, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 October 5, 2020

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  • Active Ingredient


    Isopropyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • For preparation of the skin prior to injection
    • 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
    • use only in a well ventilated area:fumes may be toxic

    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 righ away.

  • Directions

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

    Protect from freezing and avoid excessive heat.

  • Inactive Ingredient

    Water

  • PRINCIPAL DISPLAY PANEL

    Alcohol Prep Pads 50ct

    image of carton label

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PADS 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67510-0251
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67510-0251-550 in 1 BOX08/20/2013
    11 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:67510-0251-224 in 1 BOX08/20/2013
    21 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:67510-0251-440 in 1 BOX09/02/2020
    31 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/20/2013
    Labeler - Kareway Product, Inc. (121840057)
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