DESENEX- miconazole nitrate powder 
Crown Laboratories

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Desenex

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

Warnings

For external use only · Avoid contact with eyes.

Do Not Use

  • for nail or scalp infections

When using this product

  • do not get into the eyes

Stop use and ask a doctor if

  • irritation occurs or gets worse
  • no improvement within 4 weeks

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

Aldioxa, Chloroxylenol, Croscarmellose Sodium, Fragrance, Imidazolidinyl Urea, Magnesium Stearate, Microcrystalline Cellulose, Sodium Acrylates Crosspolymer-2

Questions or comments?

call 1-833-279-6522

Principal Display

NDC 0316-0225-30

New & Improved

Desenex®

Miconazole Nitrate 2% Antifungal Treatment

PRESCRIPTION STRENGTH

TRIPLE ACTION POWDER

Absorbs Wetness

Repels Moisture

Relieves Itching & Burning

Cures Most Athlete's Foot

NET WT. 3 oz (85 g)

PRODUCT PACKAGED BY WEIGHT NOT VOLUME

©2020 Crown Laboratories, Inc.

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

DESENEX is a registered trademark of Crown Laboratories, Inc.

P11528.01

desenex

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
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
IMIDUREA (UNII: M629807ATL)  
ALDIOXA (UNII: 8T66I31YNK)  
SODIUM ACRYLATES CROSSPOLYMER-2 (UNII: D3HPR4WW6F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0225-1543 g in 1 CONTAINER; Type 0: Not a Combination Product12/01/2018
2NDC:0316-0225-3085 g in 1 CONTAINER; Type 0: Not a Combination Product12/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C08/03/2009
Labeler - Crown Laboratories (079035945)

Revised: 2/2022
Document Id: d88d32bb-069b-135d-e053-2a95a90a852c
Set id: 7c4a483e-199a-7ee1-e053-2a91aa0a3dec
Version: 9
Effective Time: 20220221
 
Crown Laboratories