Miconazole Nitrate: Package Insert and Label Information

MICONAZOLE NITRATE- miconazole nitrate aerosol, powder
Wal-Mart Stores, Inc.

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.

Active ingredient

Miconazole nitrate 2%




  • cures most jock itch (linea cruris)
  • relieves symptoms of jock itch including itching, burning and chafing associated with jock itch

For external use only.


Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF

When using this product

  • do not get into eyes or mouth
  • use only as directed

Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.

​Stop use and ask a doctor if

  • irritation occurs
  • no improvement within 2 weeks for jock itch

​Keep out of reach of children.

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.


  • wash affected area and dry thoroughly
  • shake can well and spray a thin layer over affected area twice daily (morning and night) or as directed by a doctor
  • supervise children in the use of this product
  • use daily for 2 weeks, if conditions persist, consult a doctor
  • in case clogging, clear nozzle under running water
  • this product is not effective on scalp or nails

​Other information

store between 20º and 30ºC (68ºF and 86º)

​Inactive ingredients

isobutane (propellant), SD alcohol 40-B(10%w/w), stearalkonium hectorite, talc


Call 1-888-287-1915

​Principal Display Panel


Jock Itch

Powder Spray

Miconazole Nitrate 2%


Cures Most Jock Itch

  • Relieves itching, chafing and burning

NET WT 4.6 FL OZ (130 g)

Equate_Antifungal Miconazole Jock Itch Powder Spray_46-MPSWM
(click image for full-size original)
jock itch powder spray aerosol, powder
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-339
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 Multilevel Packaging
1 NDC:49035-339-46 130 g in 1 CANISTER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333C 02/25/2014
Labeler — Wal-Mart Stores, Inc. (051957769)

Revised: 12/2019 Wal-Mart Stores, Inc.

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