Label: MAXIM 50% ISOPROPYL RUBBING ALCOHOL- 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 20, 2019

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  • Drug Facts

  • Active ingredients (by volume)

    Isopropyl alcohol (50% Conc)

  • Purpose

    First aid antiseptic

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact poison control centre right away. (1-800-222-1222) 

  • INDICATIONS & USAGE

    Uses helps prevent the risk of infection in: • minor cuts • scrapes • burns

  • Warnings

    For external use only

    Flammable • keep away from fire or flame, heat, spark, electrical

    Ask a doctor before use for deep or puncture wounds, animals bites or serious burns

    When using this products • do not get into eyes • do not inhale • do not apply over large areas of the body • do not use longer than 1 week

    Stop use and ask a doctor if condition persists or gets worse

  • Directions

    • Clean affected area • spray a small amount of this product on the area 1 to 3 times daily • may be covered with sterile bandage
    • if bandaged, let dry first

  • INACTIVE INGREDIENT

    Inactive ingredient Purified water

  • STORAGE AND HANDLING

    Other information •Keep tightly closed and at controlled room temperature
    • does not contain, nor is intended as a substitute for grain or ethyl alcohol • will produce serious gastric disturbances if taken internally.

  • SPL UNCLASSIFIED SECTION

    For Rubbing & Massaging

    Made in India

    Imported by: OSTL Inc.
    5805 White Oak Ave Encino CA, 91416
    WWW.OSTLTRADE.COM

  • Packaging

    IPA 50%

  • INGREDIENTS AND APPEARANCE
    MAXIM 50% ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69950-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL50 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69950-003-02295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/17/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/17/2016
    Labeler - OSTL, INC. (020117798)
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