Label: MEDI-FIRST FIRST AID ANTISEPTIC- isopropyl alcohol spray

  • NDC Code(s): 78495-102-01
  • Packager: Ultra Distributors Inc
  • 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 December 18, 2020

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

View All Sections
  • Active ingredient

    Isopropyl Alcohol 70.0%

  • Purpose

    First aid antiseptic

  • Uses

    First aid to help prevent infection in minor cuts, scrapes, and burns

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

  • Do not use

    • near eyes or mucous membranes
    • on deep or puncture wounds, animal bites, or serious burns consult a physician
    • on large areas of the body
    • for longer than one week unless directed by a doctor
  • Stop use and ask a doctor 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.

  • Directions

    • clean affected area & spray 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
    • not to be used on children under 12 years of age

  • Inactive ingredient

    purified water

  • Questions or comments?

    1-800-634-7680

  • SPL UNCLASSIFIED SECTION

    Flammable, keep away from fire or flame.

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

    Store at 68°-77°F(20°-25°C)

  • PRINCIPAL DISPLAY PANEL

    image of bottle label

  • INGREDIENTS AND APPEARANCE
    MEDI-FIRST FIRST AID ANTISEPTIC 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78495-102
    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:78495-102-0159.1 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/19/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/19/2020
    Labeler - Ultra Distributors Inc (007160073)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!