NDC 73048-002 Zen Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
73048-002
Proprietary Name:
Zen Hand Sanitizer
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Labeler Code:
73048
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
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Product Details

What is NDC 73048-002?

The NDC code 73048-002 is assigned by the FDA to the product Zen Hand Sanitizer which is product labeled by Zen Enterprises. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 73048-002-01 100 ml in 1 bottle , 73048-002-02 200 ml in 1 bottle , 73048-002-03 500 ml in 1 bottle, pump , 73048-002-04 5000 ml in 1 jug , 73048-002-05 60 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 Zen Hand Sanitizer?

Place enough product on hands to cover your hands. Rub hands briskly until dry.No rinsing requiredNo towels needed

Which are Zen Hand Sanitizer UNII Codes?

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

Which are Zen 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 Zen 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".