DESENEX- miconazole nitrate powder 
Crown Laboratories

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Desenex

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

Warnings

For external use only.

Avoid contact with eyes.

Do not use

on children under 2 years of age unless directed by a doctor.

If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

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. If condition persists longer,
consult a doctor. This product is not effective on the scalp or nails.

Other information

Inactive ingredients

1,2-Hexanediol, Aloe Barbadensis Leaf Juice Powder, Beta-Glucan, Caprylyl Glycol, Fragrance, Glycerin, Potassium Sorbate, Sodium Benzoate, Tapioca Starch, Tricalcium Phosphate, Water, Zea Mays (Corn) Starch

Questions?

call 1-833-279-6522

Principal Display

New & Improved

Desenex®

Antifungal Foot Powder

with 2% Miconazole Nitrate

PRESCRIPTION STRENGTH

Cures Most Athlete's Foot

Triple Action Powder

Relieves Itching, Burning, and Scaling

Attacks and Absorbs Moisture

All Day Odor Control

NET WT. 1.5 oz [43g]

PRODUCT PACKAGED BY WEIGHT NOT VOLUME

©2023 Crown Laboratories, Inc.

Distributed by: Crown Laboratories, Inc . Johnson City, TN 37604

DESENEX is a registered trademark of Crown Laboratories, Inc.

P12319.00

Desenex Bottle Label

DESENEX 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0225
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
STARCH, TAPIOCA (UNII: 24SC3U704I)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
WATER (UNII: 059QF0KO0R)  
STARCH, CORN (UNII: O8232NY3SJ)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
YEAST .BETA.-D-GLUCAN (UNII: 44FQ49X6UN)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0225-0143 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/19/2023
2NDC:0316-0225-0285 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00510/19/2023
Labeler - Crown Laboratories (079035945)

Revised: 11/2023
Document Id: 09cd922d-258a-3903-e063-6394a90ae99a
Set id: 09964187-12f1-bbe6-e063-6394a90acba0
Version: 2
Effective Time: 20231110
 
Crown Laboratories