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Desenex

Dosage form: powder
Ingredients: MICONAZOLE NITRATE 2g in 100g
Labeler: GlaxoSmithKline Consumer Healthcare Holdings (US)
NDC Code: 0067-0949

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.

Drug Facts

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses
cures most athlete’s foot (tinea pedis)
relieves itching, burning, cracking and discomfort associated with athlete’s foot

Warnings

For external use only

Do Not Use
in the eyes
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
adults and children 2 years and older
wash the affected area with soap and water and dry completely before applying
apply a thin layer over affected area twice a day (morning and night) or as directed by a doctor
supervise children in the use of this product
pay special attention to the spaces between the toes. Wear well-fitting, ventilated shoes, and change shoes and socks at least once a day
use every day for 4 weeks
children under 2 years of age: ask a doctor

Other information
store at controlled room temperature 20-25°C (68-77°F)
See container bottom for lot number and expiration date

Inactive ingredients

corn starch, fragrance, talc

Questions or comments?

call 1-800-452-0051

Principal Display

NDC 0067-0949-30

Prescription Strength

Desenex®

Powder

2% Miconazole Nitrate, Antifungal

Absorbs Wetness

CURES MOST ATHLETE’S FOOT

RELIEVES ITCHING & BURNING

PRODUCT PACKAGED BY WEIGHT NOT VOLUME

NET WT. 3 oz (85 g)

Distributed by:  

GSK Consumer Healthcare

Warren, NJ 07059

©2016 GSK or its licensor.

12922

DESENEX 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-0949
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (MICONAZOLE) MICONAZOLE NITRATE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN 
TALC 
Packaging
#Item CodePackage Description
1NDC:0067-0949-1543 g in 1 CONTAINER
2NDC:0067-0949-3085 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C08/03/200907/31/2020
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) (079944263)

 
GlaxoSmithKline Consumer Healthcare Holdings (US)

Medically reviewed on Nov 16, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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