MICONAZOLE NITRATE- athletes foot powder spray talc free aerosol, powder 
Chain Drug Marketing Association

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Quality Choice Antifungal Miconazole (Athlete's Foot) Powder Spray Talc-Free

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

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 4 weeks for athlete's foot and ringworm; 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

Other information

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

Inactive ingredients

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

Questions?

call 1-866-964-0939

Principal Display Panel

Quality Choice

Talc- Free

Athlete's Foot

Antifungal Powder Spray

Miconazole Nitrate 2%

NET WT 4.6 OZ (130 g)

Quality Choice_Anti-Fungal Miconazole Powder Spray_50-031QC-01.jpg

MICONAZOLE NITRATE 
athletes foot powder spray talc free aerosol, powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-180
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE2.6 g  in 130 g
Inactive Ingredients
Ingredient NameStrength
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
ISOBUTANE (UNII: BXR49TP611)  
KAOLIN (UNII: 24H4NWX5CO)  
ALCOHOL (UNII: 3K9958V90M)  
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-180-46130 g in 1 CAN; Type 0: Not a Combination Product12/19/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00512/19/2017
Labeler - Chain Drug Marketing Association (011920774)

Revised: 2/2024
Document Id: 106b1ac0-c63c-bc9d-e063-6294a90a4f2a
Set id: edc2da26-ae46-4175-86ed-83e1a65f6d14
Version: 5
Effective Time: 20240202
 
Chain Drug Marketing Association