Label: ALCOHOL- isopropyl alcohol swab

  • NDC Code(s): 11822-5156-2, 11822-5156-6
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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  • Active ingredient

    Isopropyl alcohol 70% w/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.

    When using this product

    • do not get in the eyes or apply over large areas of the body
    • in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
    • do not use longer than 1 week unless directed by a doctor

    Stop use and ask a doctor if

    • the condition persists or gets worse

    Keep out of reach of children.

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

  • Directions

    • clean the affected area
    • discard after a 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:

    Rite Aid Corporation

    30 Hunter Lane, Camp Hill, PA 17011 USA

    Packaged in China with components of Taiwan

    REF: RA090734V1; RA090734D2

    V4 RH23LPD; V1 RJ23LPD

  • Package Label

    Packet V4 RH23LPD

    Box V4 RH23LPD

    Label V1 RJ23LPD

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-5156
    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:11822-5156-6100 in 1 BOX12/01/2011
    11 in 1 PACKET
    10.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:11822-5156-2200 in 1 BOX12/01/2011
    21 in 1 PACKET
    20.5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/01/2011
    Labeler - Rite Aid Corporation (014578892)
    Registrant - Medline Industries, LP (025460908)
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