Label: PHARMA C WIPES 70 ISOPROPYL ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 55239-327-00
  • Packager: Kleen Test Products Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2023

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

  • Drug Facts

  • Active ingredient

    Isopropyl alcohol 70%

    Purpose

    First aid antiseptic

  • Use[s]

    first aid to help prevent the risk of infection in: 

    • minor cuts • scrapes • burns

  • Warnings

    For external use only. FlammableKeep away from heat or flame.

    Will produce serious gastric disturbances if taken internally.

    Ask a doctor before use if you have

    • deep or puncture wounds • animal bites • serious burns

    When using this product

    • do not get in eyes • do not apply over large areas of the body • do not use longer than 1 week unless directed by a doctor

    Stop use and ask a doctor if

    condition persists or gets worse.

    Keep out of reach of children.

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

  • Caution

    - Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membrenes. Avoid getting this product.

  • Directions

    • clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage  • if bandaged, let dry first

  • Other information

    • does not contain, nor is intended to be a subsititute for ethyl or grain alcohol 
    • store at room temperature
  • Inactive ingredient

    purified water

  • Questions or comments?

    1-844-308-8600

  • Package Labeling:

    Label9

  • INGREDIENTS AND APPEARANCE
    PHARMA C WIPES 70 ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55239-327
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55239-327-0088 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/01/2022
    Labeler - Kleen Test Products Corporation (168165814)