Label: PUBLIX ALCOHOL- isopropyl alcohol swab

  • NDC Code(s): 56062-826-09, 56062-826-30
  • Packager: Publix Super Markets, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 22, 2023

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  • Active ingredient

    Isopropyl alcohol 70% v/v

  • Purpose

    first aid antiseptic

  • Uses

    • first aid to help prevent the risk of 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

    • clean the affected area
    • discard after single use
    • may be covered with a sterile bandage
  • 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:

    Publix Super Markets, Inc.

    Publix Corporate Pkwy, Lakeland, FL 33811 USA

    Made in China

    publix.com

    REF: PUB090734C

    V2 RK23LPD

  • Package Label

    Label V2 RK23LPD

    Box V2 RK23LPD

  • INGREDIENTS AND APPEARANCE
    PUBLIX ALCOHOL 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56062-826
    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:56062-826-30100 in 1 BOX01/01/2013
    11 in 1 PACKET
    15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:56062-826-091 in 1 PACKET01/01/2013
    25 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2013
    Labeler - Publix Super Markets, Inc. (006922009)
    Registrant - Medline Industries, LP (025460908)
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