NDC 71454-3040 Hemirus Hand Clinic Gel 62%

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:
71454-3040
Proprietary Name:
Hemirus Hand Clinic Gel 62%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
71454
Start Marketing Date: [9]
03-31-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 71454-3040?

The NDC code 71454-3040 is assigned by the FDA to the product Hemirus Hand Clinic Gel 62% which is product labeled by Gc Us Corporation. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 71454-3040-1 500 ml in 1 bottle, pump , 71454-3040-2 100 ml in 1 tube , 71454-3040-3 30 ml in 1 tube . 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 Hemirus Hand Clinic Gel 62%?

Pump as needed into your palms and throughly spread on both hands.rub into skin until dry.

Which are Hemirus Hand Clinic Gel 62% UNII Codes?

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

Which are Hemirus Hand Clinic Gel 62% 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 Hemirus Hand Clinic Gel 62%?

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".