Label: NEXXGEN 50% RUBBING ALCOHOL- isopropyl alcohol liquid

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

Drug Label Information

Updated January 3, 2024

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

  • Drug Facts

  • Active ingredients (by volume):

    Isopropyl alcohol (50% conc.)

  • Purpose

    first aid antiseptic

  • Uses

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

  • Warnings

    For external use only; flammable, keep away from fire or flame, heat, spark, electrical

    Ask a doctor before use if you have
    • deep punctured 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

    Stop using this product if
    • condition persists or gets worse

    Keep this and all drugs out of the reach of children.
    In case of accidental ingestion, seek professional assistance or contact a Poison control center (1‑800‑222‑1222) immediately.

  • Directions

    • Clean affected area
    • Apply small amount of this product on the area 1-3 times daily
    • May be covered with a sterile bandage
    • If bandaged, let dry first

  • Other information

    • store at room temperature
    • does not contain, nor is intended as a substitute for grain or ethyl alcohol. Will produce serious gastric disturbances if taken internally.

  • Inactive Ingredient

    purified water

  • SPL UNCLASSIFIED SECTION

    for Rubbing & Massaging

    Use only in a well ventilated area; Fumes may be harmful.

    TAMPER EVIDENT: DO NOT USE IF THE UNDER CAP PRINTED SAFETY FOIL IS BROKEN OR MISSING.

    Brand Owner: A&A Nexxgen LLC

    Distributed by:
    ALL CLEANERS AND MORE LLC.
    1 Passaic Street Unit 4 Wood Ridge
    NJ 07075

    Made in Jordan

  • Packaging

    rubbingalcohol50%

  • INGREDIENTS AND APPEARANCE
    NEXXGEN 50% RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83629-019
    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:83629-019-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/03/2024
    Labeler - A & A Nexxgen LLC (067596347)