DESENEX- miconazole nitrate powder 
Novartis Consumer Health, Inc.

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.

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Drug Facts

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

Warnings

For external use only

Do Not Use

When using this product

Stop use and ask a doctor if

Keep Out of Reach of Children

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

Directions

Other information

Inactive ingredients

corn starch, fragrance, talc

Questions or comments?

call 1-800-452-0051

Distributed by:  

Novartis Consumer Health, Inc.

Parsippany, NJ 07054-0622

Principal Display Panel

NDC 0067-0949-30

2% Miconazole Nitrate, Antifungal

Desenex®

Powder

Absorbs Wetness

Cures Most Athlete’s Foot

Relieves Itching & Burning

Principal Display

Desenex Shake Powder 3.0 oz label
DESENEX 
miconazole nitrate powder
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-0949
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 2 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0067-0949-15 43 g in 1 CONTAINER
2 NDC:0067-0949-30 85 g in 1 CONTAINER
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333C 08/03/2009
Labeler - Novartis Consumer Health, Inc. (879821635)

Revised: 12/2012
Document Id: c2ec4973-07d6-480f-b47a-ac57b4b703f1
Set id: c2ec4973-07d6-480f-b47a-ac57b4b703f1
Version: 1
Effective Time: 20121203
 
Novartis Consumer Health, Inc.