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  4. NDC Product Code: 60608-013 Bio-scriptives Extreme Af

NDC 60608-013 Bio-scriptives Extreme Af

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60608-013?
  4. Bio-scriptives Extreme Af Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
60608-013
Proprietary Name:
Bio-scriptives Extreme Af
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biochemics, Inc.
Labeler Code:
60608
Product Label ID:
e901c834-dcac-4d12-85f2-655ca9239cfe
Start Marketing Date: [9]
07-27-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 60608-013?

The NDC code 60608-013 is assigned by the FDA to the product Bio-scriptives Extreme Af which is product labeled by Biochemics, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60608-013-00 56.69 g in 1 bottle, pump . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Bio-scriptives Extreme Af?

■  Wash the feet and dry thoroughly.■  Apply a thin layer of product to the feet once or twice daily (morning and/or night).■  Supervise children in the use of this product.■  Pay special attention to the spaces between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily.■  Do not use if safety seal is broken.

Which are Bio-scriptives Extreme Af UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Bio-scriptives Extreme Af Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Bio-scriptives Extreme Af?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".