Label: DESENEX ANTIFUNGAL FOOT CREAM- miconazole nitrate cream
- NDC Code(s): 0316-0255-01
- Packager: Crown Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 24, 2025
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- 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-fiting, ventilated shoes, and change shoes and socks at least once daily.
- Use daily for 4 weeks. If condition persists longer consult a doctor.
- This product is not effective on the scalp or nails.
- Other information
- Inactive ingredients
- Questions?
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Desenex Cream Tube
Desenex
Antifungal Foot Cream
with 2% Miconazole Nitrate
PRESCRIPTION STRENGTH
Cures Most Athlete's Foot
Dual Action Cream
Relieves Itching, Burning, Scaling, and Discomfort
Patented Odor Control Technology
Clean Fresh Scent
NET WT. 1oz (28g)
Distributed by: Crown Laboratories, Inc. Johnson City, TN 36704
P12801.00
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Desenex Cream Carton
Desenex
Antifungal Foot Cream
with 2% Miconazole Nitrate
PRESCRIPTION STRENGTH
Cures Most Athlete's Foot
Dual Action Cream
Relieves Itching, Burning, Scaling, and Discomfort
Patented Odor Control Technology
Clean Fresh Scent
NET WT. 1oz (28g)
Distributed by: Crown Laboratories, Inc. Johnson City, TN 37604
Desenex is a registered trademark of Crown Laboratories, Inc.
P12802.00
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INGREDIENTS AND APPEARANCE
DESENEX ANTIFUNGAL FOOT CREAM
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0316-0255 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength PARAFFINUM LIQUIDUM (UNII: T5L8T28FGP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBIC ACID (UNII: X045WJ989B) WATER (UNII: 059QF0KO0R) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CETYL PALMITATE (UNII: 5ZA2S6B08X) DIPROPYLENE GLYCOL (UNII: E107L85C40) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) SORBITOL (UNII: 506T60A25R) BENZYL BENZOATE (UNII: N863NB338G) POLYSORBATE 60 (UNII: CAL22UVI4M) CETEARYL ALCOHOL (UNII: 2DMT128M1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0316-0255-01 1 in 1 CARTON 03/01/2025 1 28 g in 1 TUBE; 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 03/01/2025 Labeler - Crown Laboratories, Inc. (079035945) Establishment Name Address ID/FEI Business Operations Crown Laboratories, Inc. 079035945 manufacture(0316-0255)