Miconazole Nitrate description, usages, side effects, indications, overdosage, supplying and lots more!

Miconazole Nitrate

Premier Brands of America Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Miconazorb AF Powder


Miconazole nitrate 2%


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

For external use only.

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

​ avoid contact with the eyes

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

If swallowed, get medical help or contact a Poison Control Center right away. Do not use on children under 2 years of age unless directed by a doctor.

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

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

call 1-866-964-0939



Miconazole Nitrate 2%
Anti-fungal Powder

Cures and soothes most athlete's foot, jock itch and ringworm

  • Absorbs moisture
  • Soothes chafing, itching and burning

NET WT 2.5 OZ (71g)

Miconazole Nitrate

Miconazorb AF Powder POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:56104-020
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength

Inactive Ingredients

Ingredient Name Strength


# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:56104-020-25 71 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2013-01-01

Be sure to consult your doctor before taking any medication!
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