NDC 54708-015 Instant Hand Sanitizer

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:
54708-015
Proprietary Name:
Instant Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Venus Skin & Hair Laboratory Ltd.
Labeler Code:
54708
Start Marketing Date: [9]
05-18-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54708-015-08

Package Description: 500 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 54708-015?

The NDC code 54708-015 is assigned by the FDA to the product Instant Hand Sanitizer which is product labeled by Venus Skin & Hair Laboratory Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54708-015-08 500 ml in 1 bottle, pump . 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 Instant Hand Sanitizer?

Take 2ml of this product and directly apply it to the skin of the hand. Leave for 1 minute and let it air dry. No need to wash with water. Repeated use may cause a slight sticky feeling, can rinse with water.

Which are Instant Hand Sanitizer UNII Codes?

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

Which are Instant Hand Sanitizer 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 Instant Hand Sanitizer?

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".