Label: ANTIFUNGAL SOLUTION MAXIMUM STRENGTH- tolnaftate liquid
- NDC Code(s): 11822-9600-1
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
-
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?
-
Principal Display Panel
MAXIMUM STRENGTH
Anti-fungal Solution
Tolnaftate 1%
Proven clinically effective in the treatment of fungus on fingers, toes & skin around nails
Prevents the recurrence of most athlete's foot with daily use
Relieves itching, burning & scaling
Built-in brush for easy application
With moisturizing ingredients
SHAKE WELL BEFORE USE
1 FL. OZ. (30 mL)
-
INGREDIENTS AND APPEARANCE
ANTIFUNGAL SOLUTION MAXIMUM STRENGTH
tolnaftate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-9600 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 PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BETASIZOFIRAN (UNII: 2X51AD1X3T) EDETATE DISODIUM (UNII: 7FLD91C86K) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-9600-1 1 in 1 CARTON 03/14/2024 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 03/12/2024 Labeler - Rite Aid Corporation (014578892)