NDC 74990-700 Skm 70% Rubbing 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:
74990-700
Proprietary Name:
Skm 70% Rubbing Alcohol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
74990
Start Marketing Date: [9]
12-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 74990-700?

The NDC code 74990-700 is assigned by the FDA to the product Skm 70% Rubbing Alcohol which is product labeled by Skm Industries Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 74990-700-01 3790 ml in 1 bottle , 74990-700-12 354 ml in 1 bottle , 74990-700-16 473 ml in 1 bottle , 74990-700-32 946 ml in 1 bottle . 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 Skm 70% Rubbing Alcohol?

• clean affected area • apply a small amount of this product on the area 1 to 3 times daily • if bandaged, let dry first • may be covered with a sterile bandage

Which are Skm 70% Rubbing Alcohol UNII Codes?

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

Which are Skm 70% Rubbing 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 Skm 70% Rubbing 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".