MICONAZOLE NITRATE- anti-fungal powder miconazole nitrate talc free powder 
AmerisourceBergen Drug Corporation

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GNP Miconazorb Antifungal 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

GOOD NEIGHBOR PHARMACY

Miconazorb AF

Miconazole Nitrate 2%

ANTIFUNGAL POWDER

NET WT 2.5 OZ (71 g)

GNP_Miconazorb AF_ 50-081GN_51-081GN.jpg

MICONAZOLE NITRATE 
anti-fungal powder miconazole nitrate talc free powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-444
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)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
IMIDUREA (UNII: M629807ATL)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-444-2771 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/08/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00508/08/2017
Labeler - AmerisourceBergen Drug Corporation (007914906)

Revised: 1/2024
Document Id: 1017ca0d-3a44-6655-e063-6294a90a9819
Set id: 9cd8f0b0-1e63-4e8c-b0a0-e5da6abaf49a
Version: 5
Effective Time: 20240129
 
AmerisourceBergen Drug Corporation