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

Menu
Search

Desenex

Novartis Consumer Health, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Desenex 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

Desenex 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

Desenex ®

Powder

Absorbs Wetness

Cures Most Athlete’s Foot

Relieves Itching & Burning

Principal Display

Desenex

MICONAZOLE NITRATE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0067-0949
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE 2 g

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
talc

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0067-0949-15 43 in 1 CONTAINER
2 NDC:0067-0949-30 85 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2009-08-03


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.