Label: MEDLINE- ethyl alcohol cloth

  • NDC Code(s): 53329-842-30, 53329-842-90, 53329-842-98
  • Packager: Medline Industries, LP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 10, 2024

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

  • Active ingredient

    Alcohol 80% v/v

  • Purpose

    Antiseptic

  • Uses

    • • health care personnel hand rub to help reduce bacteria that potentially can cause disease
  • Warnings

    For external use only.

    Flammable. Keep away from heat or flame.

    Do not use

    • • in children less than 2 months of age
    • • on open skin wounds

    When using this product

    • • keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water

    Stop use and ask a doctor

    if irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children.

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

  • Directions

    • • place enough product on hands to cover all surfaces. Rub hands together until dry
    • • supervise children under 6 years of age when using this product to avoid swallowing
  • Other information

    • • store between 15-30°C (59-86°F)
    • • avoid freezing and excessive heat above 40°C (104°F)
  • Inactive ingredients

    glycerin, hydrogen peroxide, purified water USP

  • Manufacturing Information

    Manufactured by:

    Medline Industries, LP

    Three Lakes Drive, Northfield, IL 60093 USA

    Made in USA

    1-800-MEDLINE (633-5463)

    REF: HHWIPES001

    RI20HND

  • Package Label

    front

    back

  • INGREDIENTS AND APPEARANCE
    MEDLINE 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-842
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-842-981000 in 1 CASE01/01/202101/31/2022
    1NDC:53329-842-901.5 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:53329-842-30100 in 1 BOX01/01/202101/31/2022
    2NDC:53329-842-901.5 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/31/202001/31/2022
    Labeler - Medline Industries, LP (025460908)
    Registrant - Medline Industries, LP (025460908)