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Zeasorb

Physicians Total Care, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Miconazole nitrate 2%

Purpose

antifungal

Use (Athlete's Foot)

for the cure of most athlete's foot

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.

Keep out of reach of children.

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

  • 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.

Zeasorb 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.



Additional barcode labeling by:
Physicians Total Care, inc.
Tulsa, Oklahoma      74146

Principal Display Panel

NDC 54868-5876-0

Zeasorb

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)


Zeasorb

miconazole nitrate POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54868-5876(NDC:0145-1506)
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE 20.6 mg

Inactive Ingredients

Ingredient Name Strength
ACRYLAMIDE
ALDIOXA
Chloroxylenol
IMIDUREA
POWDERED CELLULOSE
talc

Product Characteristics

Color
WHITE (white to off-white)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54868-5876-0 71 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2008-03-31


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Be sure to consult your doctor before taking any medication!
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