NDC 54868-5876 Zeasorb AF

NDC Product Code 54868-5876

NDC CODE: 54868-5876

Proprietary Name: Zeasorb AF What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF-WHITE)

NDC Code Structure

  • 54868 - Physicians Total Care, Inc.

NDC 54868-5876-0

Package Description: 71 g in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Zeasorb AF with NDC 54868-5876 is a product labeled by Physicians Total Care, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1437793 and 998461.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ACRYLAMIDE (UNII: 20R035KLCI)
  • ALDIOXA (UNII: 8T66I31YNK)
  • CHLOROXYLENOL (UNII: 0F32U78V2Q)
  • IMIDUREA (UNII: M629807ATL)
  • POWDERED CELLULOSE (UNII: SMD1X3XO9M)
  • TALC (UNII: 7SEV7J4R1U)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Physicians Total Care, Inc.
Labeler Code: 54868
Start Marketing Date: 03-31-2008 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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Information for Patients

Miconazole

Miconazole is pronounced as (mi kon' a zole)

Why is miconazole medication prescribed?
Miconazole, an antifungal agent, is used for skin infections such as athlete's foot and jock itch and for vaginal yeast infections.This medication is sometimes prescribed...
[Read More]

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Zeasorb AF Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

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.

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.

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.comIRONMAN® 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

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