Label: ALCOHOL PREP PAD- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 February 20, 2023

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  • GENERAL PRECAUTIONS

    Apply topically as needed

    Discard after single use

    Saturated with 70% Isopropyl Alcohol
    Not made with natural rubber latex

    Box Front

  • Active Ingredient:

    Isopropyl Alcohol 70%v/v

  • Purpose

    Antiseptic Cleanser

  • Use:

    For preparation of the skin prior to an injection.

  • Warnings

    •For external use only
    •Flammable, keep away from fire or flame.

  • Do not use

    with electrocautery procedures

    in the eyes. If contact occurs, flush eyes with water

  • Stop use and ask a doctor if

    • redness or irritation develops.
    • If condition continues for more than 72 hours.
  • Keep out of reach of children

    •If swallowed, get medical help or contact Poison Control Center immediately.

  • Directions

    Apply alcohol as needed to clean intended area.

    Discard after single use.

  • Other Information

    Store at Room Temperature 15 - 30 C (89 - 86 F)

  • Inactive Ingredient

    Purified water.

  • 200 Pad Medium Box

    M

    Alcohol Prep

    Pad Sterile

    Apply topically as needed

    Discard after single use

    Saturated with 70% Isopropyl Alcohol
    Not made with natural rubber latex

    Content:

    200 Pad

    Medium

    NDC: 71412-110-20

    Front box

    side boxback box

    new box pre pad frontnew box alcohol prep pad back artInner Front BoxInner back box

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71412-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71412-110-20200 in 1 BOX05/26/2017
    11 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34405/26/2017
    Labeler - R&C Imports LLC (117081780)
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