Label: MEDPRIDE- isopropyl alcohol liquid

  • NDC Code(s): 52410-4096-3, 52410-4096-5, 52410-4096-7
  • Packager: Shield Line LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 17, 2024

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

  • 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

    ■ 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

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

  • 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

    MdPrdIsprpylAlc

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-4096
    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:52410-4096-3355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/01/2015
    2NDC:52410-4096-5475 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/01/2015
    3NDC:52410-4096-7946.3 mL in 1 BOTTLE; Type 0: Not a Combination Product08/23/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/01/2015
    Labeler - Shield Line LLC (078518916)