Label: WALGREEN ALCOHOL- isopropyl alcohol swab

  • NDC Code(s): 0363-0809-30, 0363-0809-60, 0363-0809-67, 0363-0809-86
  • Packager: Walgreens Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 8, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredient

    Isopropyl alcohol 70% v/v

  • Purpose

    First aid antiseptic

  • Use

    • first aid to decrease germs 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

    Questions or comments?

    1-800-633-5463

    Distributed by: Walgreen Co.

    200 Wilmot Rd., Deerfield, IL 60015

    walgreens.com

    Made in China

    WRX155524V2

    V1 RH23SXM

  • Package Label

    Packet V1 RH23SXM

    Box V1 RH23SXM

  • INGREDIENTS AND APPEARANCE
    WALGREEN ALCOHOL 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0809
    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:0363-0809-30100 in 1 BOX01/01/2011
    11 in 1 PACKET
    15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:0363-0809-67120 in 1 BOX01/01/201112/31/2019
    21 in 1 PACKET
    25 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    3NDC:0363-0809-60200 in 1 BOX01/01/2011
    31 in 1 PACKET
    35 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    4NDC:0363-0809-86400 in 1 BOX01/01/2011
    41 in 1 PACKET
    45 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2011
    Labeler - Walgreens Company (008965063)
    Registrant - Medline Industries, LP (025460908)