Label: ISOPROPYL ALCOHOL liquid

  • NDC Code(s): 0869-0810-08, 0869-0810-43, 0869-0810-45, 0869-0810-72, view more
    0869-0810-99
  • Packager: Vi-Jon, LLC
  • 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 20, 2023

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 the risk of infection in:

    • minor cuts
    • scrapes
    • burns
  • Warnings

    For external use only. If taken internally serious gastric disturbances will result.

    Flammable. Keep away from fire or flame, heat, spark, electrical

  • Ask a doctor before use

    for deep or puncutre wounds, animal bites or serious burns

  • When using this product

    • do not get into eyes
    • do not inhale
    • do not apply over large areas of the body
    • do not use longer than 1 week
  • Stop use and ask a doctor if 

    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.

  • Caution

    Fumes can be acutely irritating to skin, eyes and the respirtory system. Do not apply to irritated skin of if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product                                                                                                                                                                                                                                                            

  • Directions

    • clean the affected area
    • apply a small amount of this product on the area 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • other information

    • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • inactive ingredient

    water

  • SPL UNCLASSIFIED SECTION

    Distributed by: Vi-Jon, LLC

    8515 Page Ave.

    St. Louis, MO 63114

  • principal display panel

    NDC 0869-0810-45

    SWAN

    70% Isopropyl Alcohol

    • First Aid Antseptic
    • For Rubbing & Massaging

    Square bottle uses less plastic than a similarly sized bottle Recyclable (if available in your area)

    WARNING FLAMMABLE-Keep away from heat, spark, electrical fire or flame

    CAUTION: Do not point at self or other; product will squirt when squeezed.

    Use only in a well-ventilated area: fumes can be harmful

    32 FL OZ (1 QT) 946 mL

    image description

  • principal display panel

    mountain falls

    body rub

    for treatment of minor cuts and abrasions

    topical antiseptic & sanitizer

    massage

    70% isopropyl alcool

    first aid antiseptic

    WARNING FLAMMABLE - Keep away from heat, spark, electrical, fire or flame

    Use only in a well-ventilated area; fumes can be harmful

    Caution: Do not point at self or others; product will squirt when squeezed.

    32 FL OZ (1 QT) 946 mL

    image description

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0869-0810
    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:0869-0810-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/1989
    2NDC:0869-0810-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/1989
    3NDC:0869-0810-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/1989
    4NDC:0869-0810-99237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/1989
    5NDC:0869-0810-72295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/15/1989
    Labeler - Vi-Jon, LLC (790752542)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(0869-0810)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(0869-0810)