MICONAZOLE NITRATE- anti-fungal powder miconazole nitrate talc free powder 
Premier Brands of America Inc.

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Premier Brands Miconazorb Anti Fungal Powder - Talc Free

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

for the cure of most athlete's foot, jock itch and ringworm

Warnings

For external use only.

Do not use

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

When using this product

avoid contact with the eyes

Stop and ask a doctor if

irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 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

Inactive ingredients

allantoin, chloroxylenol, fragrance, imidazolidinyl urea, microcrystalline cellulose, tricalicum phosphate, zea mays (corn) starch

Questions?

call 1-866-964-0939

Principal Display Panel

Premier

Miconazorb AF

Miconazole Nitrate 2%

Talc-Free

NET WT 2.5 OZ (71 g)

Miconazorb Anti-Fungal

MICONAZOLE NITRATE 
anti-fungal powder miconazole nitrate talc free powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56104-039
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE1.42 g  in 71 g
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN (UNII: 344S277G0Z)  
IMIDUREA (UNII: M629807ATL)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:56104-039-2571 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/03/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00504/03/2017
Labeler - Premier Brands of America Inc. (117557458)

Revised: 2/2024
Document Id: 10562801-375d-80b5-e063-6394a90a5c89
Set id: 5df6fef0-4e3d-9cb8-e053-2a91aa0a21e5
Version: 5
Effective Time: 20240201
 
Premier Brands of America Inc.