Label: LIQUID ANTIFUNGAL TREATMENT- tolnaftate liquid

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

Drug Label Information

Updated April 1, 2024

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

View All Sections
  • ​Active ingredient

    Tolnaftate 1%

  • ​Purpose

    Antifungal

  • Uses

    for the treatment of athlete’s foot (tinea pedis) and ringworm (tinea corporis)

    for effective relief of itching, scaling, cracking, burning and redness.

  • Warnings

    For external use only.

    Flammable

    keep away from fire or flame.

    Do not use

    on children under 2 years of age unless directed by a doctor.

    When using this product

    avoid contact with the eyes.

    Stop use and consult a doctor if

    • irritation occurs or if there is no improvement within 4 weeks

    Keep out of reach of children.

    If swallowed, get medical help, or contact a Poison Control Center right away.

  • ​Directions

    • wash the affected area and dry thoroughly.
    • apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor.
    • supervise children in the use of this product.
    • for athlete’s foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
    • for athlete’s foot and ringworm, use daily for 4 weeks.
    • if condition persists longer, consult a doctor.
    • this product is not effective on the scalp or nails.

  • ​Other information​

    • Store at room temperature 15°-30°C (59° - 86°F)
    • Keep tightly closed when not in use
  • ​Inactive ingredient

    Acetone, Water, Propylene Glycol, Tocopherol Acetate.

  • Questions?

    Call 1-866-964-0939

  • Principal Display Panel

    cartonlabelComfort zone

    liquid antifungal treatment

    with vitamin e to moisturize

    TOLNAFTATE 1%/ANTIFUNGAL

    Maxiumum Strength

    Brush- On Applicator

    SHAKE WELL BEFORE USE

    1 FL. OZ. (30 mL)

  • INGREDIENTS AND APPEARANCE
    LIQUID ANTIFUNGAL TREATMENT 
    tolnaftate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72446-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACETONE (UNII: 1364PS73AF)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72446-012-011 in 1 CARTON03/29/2024
    130 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00503/29/2024
    Labeler - Hudson Health LLC (081276171)
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!