NDC 50730-8672 Ethyl Alcohol

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:
50730-8672
Proprietary Name:
Ethyl Alcohol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H And P Industries, Inc. Dba Triad Group
Labeler Code:
50730
Start Marketing Date: [9]
11-17-1997
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50730-8672-0

Package Description: 72 PACKET in 1 BOX / 5 g in 1 PACKET

Product Details

What is NDC 50730-8672?

The NDC code 50730-8672 is assigned by the FDA to the product Ethyl Alcohol which is product labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50730-8672-0 72 packet in 1 box / 5 g in 1 packet. 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 Ethyl Alcohol?

Place a palmful of product in one hand.Spread on both hands and rub into skin until dry (approx. 1-2 min.).Place a smaller amount into one hand.Spread over hands to wrist and rub into skin until dry

Which are Ethyl Alcohol UNII Codes?

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

Which are Ethyl Alcohol 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 Ethyl Alcohol?

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".