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Medically reviewed on December 4, 2017.

Dosage form: powder
Ingredients: MICONAZOLE NITRATE 2g in 100g
Labeler: Novartis Consumer Health, Inc.
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%



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


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.

  • 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 20-25C (68-77F)
  • See container bottom for lot number and expiration date

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



Absorbs Wetness

Cures Most Athlete’s Foot

Relieves Itching & Burning

Principal Display
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
Inactive Ingredients
Ingredient NameStrength
#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 finalpart333C08/03/2009
Labeler - Novartis Consumer Health, Inc. (879821635)

Novartis Consumer Health, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.