Label: ANTIFUNGAL LIQUID- tolnaftate liquid
- NDC Code(s): 56104-902-01
- Packager: Premier Brands of America Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- clean the affected area and dry thoroughly
- apply a thin layer of the product over the 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
- to prevent athlete's foot: wash the feet and dry thoroughly; apply a thin layer of the product to the feet once or twice daily (morning and/or night)
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredient
- Questions?
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Principal Display Panel
premier
solutions
Maximum Strength
ANTIFUNGAL
LIQUID
TOLNAFTATE 1%/
ANTIFUNGAL
PROVEN CLINICALLY
EFFECTIVE IN THE
TREATMENT OF FUNGUS
ON FINGERS, TOES AND
SKIN AROUND NAILS
Prevents the recurrence
of most athlete's foot with
daily use
Relieves itching,
scaling & burning
With moisturizing
ingredients
SHAKE WELL
BEFORE USE
1 FL. OZ. (30 mL)
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INGREDIENTS AND APPEARANCE
ANTIFUNGAL LIQUID
tolnaftate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56104-902 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 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EDETATE DISODIUM (UNII: 7FLD91C86K) PHENOXYETHANOL (UNII: HIE492ZZ3T) BETASIZOFIRAN (UNII: 2X51AD1X3T) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56104-902-01 1 in 1 CARTON 11/06/2024 1 30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 11/06/2024 Labeler - Premier Brands of America Inc (063849780)