Label: DR.SCHOLL S ODOR X ATHLETE S FOOT- tolnaftate cream
- NDC Code(s): 73469-0618-1
- Packager: Scholl's Wellness Company LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 14, 2026
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Uses
- Warnings
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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
- Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
- Use daily for 4 weeks
- Other information
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Inactive ingredients
Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Ceteareth-20, Cetearyl Alcohol, Chlorphenesin, Citric Acid, C13-14 Isoparaffin, Dimethicone, Disodium EDTA, Ethylhexyl Palmitate, Eucalyptus Globulus Leaf Oil, Parfum (Fragrance), Glyceryl Stearate, 1,2-Hexanediol, Hydrogenated Palm Kernel Oil, Hydroxyacetophenone, Lactobacillus Ferment, Laureth-7, Lavandula Angustifolia (Lavender) Oil, PEG-8, PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Tetrasodium Etidronate, Tetrasodium Iminodisuccinate, Vanillin, Water (Aqua, Eau), Xanthan Gum, Zinc Ricinoleate
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INGREDIENTS AND APPEARANCE
DR.SCHOLL S ODOR X ATHLETE S FOOT
tolnaftate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73469-0618 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 POLYACRYLAMIDE (CROSSLINKED; 0.01-0.2 MOLE PERCENT BISACRYLAMIDE) (UNII: RHA9LWJ494) LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP) CETEARETH-20 (UNII: YRC528SWUY) SHEA BUTTER (UNII: K49155WL9Y) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETEARYL ALCOHOL (UNII: 2DMT128M1S) CHLORPHENESIN (UNII: I670DAL4SZ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYL PALMITATE (UNII: 2865993309) EUCALYPTUS GLOBULUS LEAF OIL (UNII: 2R04ONI662) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) LAURETH-7 (UNII: Z95S6G8201) LAVENDER OIL (UNII: ZBP1YXW0H8) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PEG-100 MONOSTEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4) TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635) VANILLIN (UNII: CHI530446X) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) ZINC RICINOLEATE (UNII: BOH1Z111J2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73469-0618-1 1 in 1 CARTON 02/15/2026 1 28.3 g in 1 BOTTLE; 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 02/15/2026 Labeler - Scholl's Wellness Company LLC (117174744)


