Zeasorb

Dosage form: powder
Ingredients: MICONAZOLE NITRATE 20.6mg in 1g
Labeler: Stiefel Laboratories Inc
NDC Code: 0145-1506

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.

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.
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

Product settles during shipment. Package contains full net weight.

Inactive ingredients

acrylamide/sodium acrylate copolymer, aldioxa, chloroxylenol, fragrance, imidurea, microporous cellulose, talc. Contains no starch.

Questions?

call 1-888-438-7426. Side effects should be reported to this number.

Manufactured for: Stiefel Laboratories, Inc. Research Triangle Park, NC 27709

www.zeasorb.com

IRONMAN® is a registered trademark of World Triathlon Corporation used herein by permission.

ZEASORB is a registered trademark of Stiefel Laboratories, Inc.

Principal Display Panel

NDC 0145-1506-05

Zeasorb®

ANTIFUNGAL TREATMENT

Miconazole Nitrate 2%

Super Absorbent Powder

cures most

athlete's foot

Relieves:

Itching
Burning
Scaling

Official Partner IRONMAN®

Net Wt. 2.5 Oz (71g)

STL0000041

STL0000042

Principal Display Panel

NDC 0145-1501-03

Zeasorb®

ANTIFUNGAL TREATMENT

Miconazole Nitrate 2%

Super Absorbent Powder

cures most

jock itch

Relieves:

Itching
Burning
Scaling

Official Partner IRONMAN®

Net Wt. 2.5 Oz (71g)

STL0000043

STL0000044

ZEASORB 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0145-1506
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (MICONAZOLE) MICONAZOLE NITRATE20.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ACRYLAMIDE 
ALDIOXA 
CHLOROXYLENOL 
IMIDUREA 
POWDERED CELLULOSE 
TALC 
Product Characteristics
ColorWHITE (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:0145-1506-0571 g in 1 BOTTLE
2NDC:0145-1506-0120 POUCH in 1 CARTON
2NDC:0145-1506-612.8 g in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C03/14/2011
ZEASORB 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0145-1501
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (MICONAZOLE) MICONAZOLE NITRATE20.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ACRYLAMIDE 
ALDIOXA 
CHLOROXYLENOL 
IMIDUREA 
POWDERED CELLULOSE 
TALC 
Product Characteristics
ColorWHITE (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:0145-1501-0371 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C03/14/2011
Labeler - Stiefel Laboratories Inc (808842343)

Revised: 04/2013
 
Stiefel Laboratories Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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