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Miconazole Nitrate by Topco Associates LLC

Dosage form: powder
Ingredients: MICONAZOLE NITRATE 1.42g in 71g
Labeler: Topco Associates LLC
NDC Code: 36800-071

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.

Anti - Fungal Powder

Active ingredient

Miconazole nitrate 2%




for the cure of most athlete's foot, jock itch and ringworm


For External use only.

Do not use

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

when using this product

avoid contact with the eyes

Stop and ask a doctor if

irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

  • clean the affected area and dry thoroughly
  • apply a thin layer of product over affected area twice daily (morning and night) or as directed by a doctor
  • supervise children in the use of this product
  • for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
  • for athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks
  • if conditions persist longer, consult a doctor
  • this product is not effective on the scalp or nails

Other Information
  • store between 59º - 86ºF
  • lightly shake bottle to loosen settled powder

Inactive ingredients

aldioxa, chloroxylenol, fragrance, imidurea, powdered cellulose, talc


Call 1-888-423-0139

Principal Display Panel




Miconazole Nitrate 2%

  • Cures and soothees most athlete's foot, jock itch & ringworm
  • Relieves chafing, itching, burning & scaling
  • Absorbs moisture

COMPARE TO ZEASORB active ingredients

NET WT 2.5 OZ (71g)

anti-fungal powder miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-071
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:36800-071-2571 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C04/01/2016
Labeler - Topco Associates LLC (006935977)

Revised: 01/2016
Topco Associates LLC

← See all Miconazole Nitrate brands

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.