ZEASORB- miconazole nitrate powder 
Stiefel Laboratories Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Use (Athlete's Foot)

for the cure of most athlete's foot

Use (Jock Itch)

for the cure of most jock itch

Warnings

For external use only

Do not use

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

Avoid contact with the eyes.

Stop use and ask a doctor if (Athlete's Foot)

irritation occurs or there is no improvement within 4 weeks.

Stop use and ask a doctor if (Jock Itch)

irritation occurs or there is no improvement within 2 weeks.

Keep out of reach of children.

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

Directions (Athlete's Foot)

clean the affected area and dry thoroughly
apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
supervise children in the use of this product
pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
use daily for 4 weeks
if condition persists longer, consult a doctor
this product is not effective on the scalp or nails

Directions (Jock Itch)

clean the affected area and dry thoroughly.
apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Avoid open wounds.
supervise children in the use of this product.
use daily for 2 weeks.
if condition persists longer, consult a doctor.
this product is not effective on the scalp or nails.

Other information

Store below 25°C (77°F). Product settles during shipment. Package contains full net weight.

Inactive ingredients

aldioxa, chloroxylenol, fragrance, imidurea, powdered cellulose, sodium polyacrylate, talc

Questions?

call 1-888-438-7426

Distributed by: Stiefel Laboratories, Inc., Research Triangle Park, NC 27709

Made in India

Trademarks are owned by or licensed to the GSK group of companies.

Principal Display Panel

NDC 0145-1506-05

Super Absorbent Powder

Zeasorb® AF

ANTIFUNGAL TREATMENT

Miconazole Nitrate 2%

Super Absorbent Powder

cures most athlete's foot

Relieves:

Itching
Burning
Scaling

#1 Dermatologist Recommended

Stiefel

Net wt. 2.5 OZ (71 g)

©2015 GSK or its licensor. All rights reserved.

Front Label: 103580XC

103580XC_Zeasorb Athlete's Foot_2.5 oz.jpg

Principal Display Panel

NDC 0145-1501-03

Super Absorbent Powder

Zeasorb® AF

ANTIFUNGAL TREATMENT

Miconazole Nitrate 2%

cures most jock itch

Relieves:

Itching
Burning
Scaling

#1 Dermatologist Recommended

Stiefel

Net wt. 2.5 OZ (71 g)

©2015 GSK or its licensor. All rights reserved

Front Label: 103658XB

103658XB_Zeasorb Jock Itch_2.5 oz.jpg
ZEASORB 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0145-1506
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALDIOXA (UNII: 8T66I31YNK)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
IMIDUREA (UNII: M629807ATL)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorWHITE (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0145-1506-0571 g in 1 BOTTLE; Type 0: Not a Combination Product03/14/201105/31/2020
2NDC:0145-1506-0120 in 1 CARTON03/14/201105/31/2020
2NDC:0145-1506-612.8 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C03/14/201105/31/2020
ZEASORB 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0145-1501
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALDIOXA (UNII: 8T66I31YNK)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
IMIDUREA (UNII: M629807ATL)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorWHITE (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0145-1501-0371 g in 1 BOTTLE; Type 0: Not a Combination Product03/14/201105/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C03/14/201105/31/2020
Labeler - Stiefel Laboratories Inc (808842343)

Revised: 11/2018
 
Stiefel Laboratories Inc