Label: ALCOHOL EXTRA-THICK- isopropyl alcohol swab

  • NDC Code(s): 41250-040-81, 41250-040-82
  • Packager: Meijer Distribution Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 22, 2023

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

  • Active ingredient

    Isopropyl alcohol 70% v/v

  • Purpose

    First aid antiseptic

  • Uses

    • • first aid antiseptic 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 persists or gets worse or lasts 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

    • • protect from freezing and avoid excessive heat
    • • not made with natural rubber latex
  • Inactive ingredients

    water

  • Manufacturing information

    Distributed by:

    Meijer Distribution, Inc.

    2929 Walker Ave NW, Grand Rapids, MI 49544 USA

    Made in China with componets from Taiwan

    www.meijer.com

    REF: MJ090734SCV2

    V1 RI23SXM

  • Package Label

    Label V1 RI23SXM

    Box V1 RI23SXM

  • INGREDIENTS AND APPEARANCE
    ALCOHOL  EXTRA-THICK
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-040
    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:41250-040-81100 in 1 BOX04/06/2011
    11 in 1 PACKET
    15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:41250-040-82140 in 1 BOX04/06/2011
    21 in 1 PACKET
    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 DrugM00304/06/2011
    Labeler - Meijer Distribution Inc (006959555)
    Registrant - Medline Industries, LP (025460908)