Label: ALCOHOL CLEANSING PAD- isopropyl alcohol liquid

  • 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 December 5, 2019

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  • Active Ingredient

    Active Ingredient:                                

    Isopropyl Alcohol, 70% v/v

  • Purpose

    Antiseptic

  • Use

     For preparation of skin before injection.

  • Warnings

     For external use only.  

  • STORAGE AND HANDLING

    Flammable - keep away from fire or flame

    Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

  • DO NOT USE

    Do not use: with electrocautery, in the eyes.

  • STOP USE

    Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  If swallowed,

    get medical help or contact a Poison Control

    Center right away.

  • Directions

    Wipe Injection site vigorously and discard.

  • Inactive Ingredient

    Purified water.

  • SPL UNCLASSIFIED SECTION

    LOT/EXP:            Made in CHINA

    20140301

  • PRINCIPAL DISPLAY PANEL

    Alcohol Cleansing Pad

    Genuine First Aid LLC, Clearwater FL 33755

    www.GenuineFirstAid.com

    1/pouch

    GENUINE FIRST AID


    100 Alcohol cleansing pads

    Reorder GFAP-39-02

  • PRINCIPAL DISPLAY PANEL

    Alcohol Cleansing Pad

  • PRINCIPAL DISPLAY PANEL

    Alcohol Cleansing Pad

  • PRINCIPAL DISPLAY PANEL

    Alcohol Cleansing Pad

  • PRINCIPAL DISPLAY PANEL

    Alcohol Cleansing Pad

  • INGREDIENTS AND APPEARANCE
    ALCOHOL CLEANSING PAD 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52124-0002
    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:52124-0002-10.5 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug04/23/2010
    2NDC:52124-0002-2100 in 1 CARTON04/23/2010
    20.5 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
    3NDC:52124-0002-310 in 1 BOX04/23/2010
    30.5 mL in 1 PACKET; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/23/2010
    Labeler - Genuine First Aid LLC (619609857)
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