MICONAZOLE NITRATE- antifungal liquid continuous spray aerosol, spray 
Chain Drug Consortium, LLC

----------

Premier Value Antifungal Liquid Continuous Spray

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

Warnings

For external use only.

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

When using this product

  • avoid contact with the eyes or mouth
  • use only as directed

Stop use and ask a doctor if

  • no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch
  • irritation occurs

Do not use

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

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

Inactive ingredients

acetone, ethoxyglycol, propylene glycol, SD alcohol 40-B (74%w/w), tocopheryl acetate

Questions?

call 1-866-964-0939

Principal Display Panel

Premier Value

Medicated

Antifungal Liquid Continuous Spray

Miconazole Nitrate 2%

Net WT 5.3 OZ (150 g)

PV Antifngl Mic Nitrate LiqSpry-3.jpg

MICONAZOLE NITRATE 
antifungal liquid continuous spray aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-516
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE3 g  in 150 g
Inactive Ingredients
Ingredient NameStrength
ACETONE (UNII: 1364PS73AF)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALCOHOL (UNII: 3K9958V90M)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-516-00150 g in 1 CAN; Type 0: Not a Combination Product01/05/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00501/05/2010
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2024
Document Id: 106aa7ef-3231-a759-e063-6294a90a66c8
Set id: 7f6912a6-a576-4138-bd78-a075a7d24036
Version: 9
Effective Time: 20240202
 
Chain Drug Consortium, LLC