Label: ALCOHOL- isopropyl alcohol swab

  • NDC Code(s): 30142-809-30, 30142-809-31
  • Packager: The Kroger Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • Active ingredient

    Isopropyl alcohol 70% v/v

  • Purpose

    First aid antiseptic

  • Uses

    • first aid to help prevent infection 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

    • do not flush
    • protect from freezing and avoid excessive heat
    • not made with natural rubber latex
  • Inactive Ingredients

    water

  • Manufacturing Information

    Distributed by:

    The Kroger Co.

    1014 Vine Street, Cincinnati, OH 45202

    Packaged in China with components of Taiwan

    800-632-6900

    www.kroger.com

    REF: KGR090731CV2

    V1 RK22LPD

  • Package Label

    Box V1 RK22LPD

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-809
    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:30142-809-30100 in 1 BOX03/31/2010
    11 in 1 PACKET
    10.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:30142-809-31140 in 1 BOX03/31/2010
    21 in 1 PACKET
    21.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/31/2010
    Labeler - The Kroger Company (006999528)
    Registrant - Medline Industries, LP (025460908)
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