NDC 49035-987 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:
49035-987
Proprietary Name:
Undecylenic Acid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wal-mart Stores Inc
Labeler Code:
49035
Start Marketing Date: [9]
06-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49035-987-74

Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 49035-987?

The NDC code 49035-987 is assigned by the FDA to the product Undecylenic Acid which is product labeled by Wal-mart Stores Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49035-987-74 1 bottle, with applicator in 1 carton / 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?

Section from Directions portion of carton label follows:Directions- Using soap and water, 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. - Use the brush applicator provided for easy application to the affected area- For toe usage, change shoes and socks at least once daily and wear well fitting, ventilated shoes- Pay particular attention to spaces between the toes for athletes foot- For athletes foot and ringworm, use the product daily for 4 weeks. If condition persists longer, consult a physician- This product is not effective on the scalp or nails- Children must be supervised in the use of this product

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:

What is the NDC to RxNorm Crosswalk for Undecylenic Acid?

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".