Label: MEDPRIDE WITH WINTERGREEN OIL- isopropyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 17, 2024

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  • Active ingredient

    Isopropyl Alcohol 70%

  • 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

    ■ will produce serious gastric disturbances if taken internally

  • 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 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

    In case of an accidental ingestion, get medical help or contact a Poison Control Center immediately

  • Directions

    ■ clean affected area ■ apply 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

    ■ does not contain, nor is intended as a substitute for grain or ethyl alcohol ■ keep bottle tightly closed

  • Inactive Ingredient

    FDC Blue 1, FDC Yellow 5, Laneth-75, Methyl Salicylate, Water

  • Package  Label

    image description

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE  WITH WINTERGREEN OIL
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-4097
    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
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52410-4097-3355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/01/2015
    Labeler - Shield Line LLC (078518916)
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