NDC 79505-012 Enviromed 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:
79505-012
Proprietary Name:
Enviromed Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unysource Enterprise
Labeler Code:
79505
Start Marketing Date: [9]
07-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 79505-012-01

Package Description: 20 mL in 1 POUCH

NDC Code 79505-012-02

Package Description: 60 mL in 1 BOTTLE, DISPENSING

NDC Code 79505-012-03

Package Description: 250 mL in 1 BOTTLE, DISPENSING

NDC Code 79505-012-04

Package Description: 500 mL in 1 BOTTLE, DISPENSING

NDC Code 79505-012-05

Package Description: 1000 mL in 1 BOTTLE

NDC Code 79505-012-06

Package Description: 4000 mL in 1 JAR

Product Details

What is NDC 79505-012?

The NDC code 79505-012 is assigned by the FDA to the product Enviromed Hand Sanitizer which is product labeled by Unysource Enterprise. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 79505-012-01 20 ml in 1 pouch , 79505-012-02 60 ml in 1 bottle, dispensing , 79505-012-03 250 ml in 1 bottle, dispensing , 79505-012-04 500 ml in 1 bottle, dispensing , 79505-012-05 1000 ml in 1 bottle , 79505-012-06 4000 ml in 1 jar . 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 Enviromed Hand Sanitizer?

Apply small amount to wetted hands and wash vigorously for 15 seconds, make sure to get between fingers and under finger nails. Rinse with warm, clean water. Repeat as necessary.  Apply small amount to wetted hands and wash vigorously for 15 seconds, make sure to get between fingers and under finger nails. Rinse with warm, clean water. Repeat as necessary. Apply small amount to wetted hands and wash vigorously for 15 seconds, make sure to get between fingers and under finger nails. Rinse with warm, clean water. Repeat as necessary. Apply small amount to wetted hands and wash vigorously for 15 seconds, make sure to get between fingers and under finger nails. Rinse with warm, clean water. Repeat as necessary. Apply small amount to wetted hands and wash vigorously for 15 seconds, make sure to get between fingers and under finger nails. Rinse with warm, clean water. Repeat as necessary. Apply small amount to wetted hands and wash vigorously for 15 seconds, make sure to get between fingers and under finger nails. Rinse with warm, clean water. Repeat as necessary.

Which are Enviromed Hand Sanitizer UNII Codes?

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

Which are Enviromed 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 Enviromed 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".