Label: TOLNAFTATE- antifungal powder spray with baking soda aerosol, powder
- NDC Code(s): 82442-402-01
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2025
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Extremely Flammable:
Keep away from fire, sparks and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF.
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Directions
- wash affected area and dry thoroughly
- shake can well and spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
- to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night)
- 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 conditions persist longer, consult a doctor
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredient
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
TOLNAFTATE
antifungal powder spray with baking soda aerosol, powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82442-402 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) ISOBUTANE (UNII: BXR49TP611) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ALCOHOL (UNII: 3K9958V90M) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82442-402-01 113 g in 1 CAN; Type 0: Not a Combination Product 06/02/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 05/31/2025 Labeler - Target Corporation (006961700)

