Label: MEDPRIDE 99% 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 January 13, 2022

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  • Active ingredient

    Isopropyl Alcohol 99%

  • Purpose

    First Aid Antiseptic

  • Uses

    first aid to help prevent risk of infection in minor cuts, scrapes and burns

  • Warnings

    For external use only

    ■ Flammable,keep away from fire and flame, heat spark or electricity

    ■ if taken internally, serious gastric disturbances will result

  • Ask a doctor before use if you have

    ■ deep or puncture wounds, animal bites or serious burns

  • When using this product

    ■ do not get into your eyes ■ do not apply over large areas of the body ■ do not use longer than one week unless directed by a doctor

    ■ do not use otherwise than directed

  • 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.

  • Directions

    ■ clean affected area ■ apply a small amount of this product on the area 1 to 3 times daily

    ■ if bandaged, let dry first ■ may be covered with a sterile bandage

  • Other information

    ■ store at room temperature

    ■ does not contain nor is intended as a substitute for grain or ethyl alcohol

  • Inactive Ingredient

    purified water

  • PRINCIPAL DISPLAY PANEL

    Principal & Drug Fact Panel

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE 99% RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-4098
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL99 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52410-4098-5475 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/08/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/08/2019
    Labeler - Shield Line LLC (078518916)
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