Label: ISOPROPYL RUBBING ALCOHOL 70%- isopropyl alcohol liquid

  • NDC Code(s): 75983-008-01, 75983-008-02, 75983-008-03, 75983-008-04, view more
    75983-008-05, 75983-008-06, 75983-008-07
  • Packager: First Aid Research Corp.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient (by volume)

    Isopropyl Alcohol (70%)

  • PURPOSE

    Purpose

    First Aid Antiseptic

  • INDICATIONS & USAGE

    Uses

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

    Warnings

    For external use only

    • Flammable, keep away from fire and flame
    • if taken internally, serious gastric disturbances will result
  • ASK DOCTOR

    Ask a doctor before use if you have

    • deep or puncture wounds, animal bites or serious burns
  • WHEN USING

    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

    Stop use and ask a doctor if

    • condition persists or gets worse
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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

  • DOSAGE & ADMINISTRATION

    Directions

    • clean effected 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
  • SPL UNCLASSIFIED SECTION

    Other information

    • store at room temperature
    • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • INACTIVE INGREDIENT

    Inactive Ingredient

    Purified Water

  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL

    ISOPROPYL RUBBING ALCOHOL 70%
    FIRST AID ANTISEPTIC
    12 FL.OZ (355 mL)

    label

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL RUBBING ALCOHOL 70% 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75983-008
    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:75983-008-01118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    2NDC:75983-008-02177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    3NDC:75983-008-03237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    4NDC:75983-008-04296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    5NDC:75983-008-05355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    6NDC:75983-008-06414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    7NDC:75983-008-07473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/10/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/10/2020
    Labeler - First Aid Research Corp. (089405927)
    Registrant - Jell Pharmaceuticals Pvt. Ltd. (726025211)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jell Pharmaceuticals Pvt. Ltd.726025211manufacture(75983-008)
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