MICONAZOLE NITRATE- jock itch powder spray aerosol, powder

Miconazole Nitrate by

Drug Labeling and Warnings

Miconazole Nitrate by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Miconazole nitrate 2%

​ ​Purpose

Antifungal

Uses

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

WARNINGS

For external use only.

Flammable:

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.

​Directions

• 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

​ ​Questions?

Call 1-888-287-1915

​Principal Display Panel

Equate

Jock Itch

Powder Spray

Miconazole Nitrate 2%

Antifungal

Cures Most Jock Itch

• Relieves itching, chafing and burning

NET WT 4.6 FL OZ (130 g)

INGREDIENTS AND APPEARANCE

MICONAZOLE NITRATE 
jock itch powder spray aerosol, powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-339
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	2.6 g  in 130 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ISOBUTANE (UNII: BXR49TP611)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
TALC (UNII: 7SEV7J4R1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-339-46	130 g in 1 CANISTER; Type 0: Not a Combination Product	02/25/2014

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)