NDC 11673-259 Undecylenic Acid

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11673-259
Proprietary Name:
Undecylenic Acid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Start Marketing Date: [9]
06-01-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11673-259-30

Package Description: 30 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 11673-259?

The NDC code 11673-259 is assigned by the FDA to the product Undecylenic Acid which is product labeled by Target Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11673-259-30 30 ml in 1 bottle, with applicator . 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 Undecylenic Acid?

Read all warnings and directions. Use only as directed.clean the affected area and dry thoroughlyapply a thin layer of the product over the affecter area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot: pay special attention to spaces between toeswear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete's foot and ringworm, use daily for 4 weeks. If conditions persists longer, consult a doctorthis product is not effective on the scalp or nails

Which are Undecylenic Acid UNII Codes?

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

Which are Undecylenic Acid 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:

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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".