Label: WALGREEN ALCOHOL- isopropyl alcohol swab

  • NDC Code(s): 0363-0809-30, 0363-0809-60, 0363-0809-67
  • Packager: Walgreens Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 September 27, 2022

If you are a consumer or patient please visit this version.

  • Active ingredient

    Isopropyl alcohol 70% v/v

  • Purpose

    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.

    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 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

    • • 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

    WRX155524V1

    RA20LPD

  • Package Label

    Package Label

  • 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
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2011
    Labeler - Walgreens Company (008965063)
    Registrant - Medline Industries, LP (025460908)