Label: ALCOHOL PREP- isopropyl alcohol patch

  • NDC Code(s): 69771-003-00
  • Packager: Geri-Gentle Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active Ingredients

    Isopropyl Alcohol 70%

    Purpose

    Antiseptic

  • Use

    For preparation of the skin prior to 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

    If irritation and redness develop. If condition continues, consult your health care practitioner.

    Keep out of reach of children.

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

  • Directions

    • Wipe injection area and discard.
  • Other information

    Store at room temperature 15 C~30 C(59 F~86 F)

  • Inactive Ingredients

    Water

  • Package Labeling:

    123

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP 
    isopropyl alcohol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69771-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69771-003-00200 in 1 BOX04/05/2017
    17 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/05/2017
    Labeler - Geri-Gentle Corporation (080367686)
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