NDC 50536-103 Alcohol Wipes

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:
50536-103
Proprietary Name:
Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
American Chemical And Sanitary Supply Inc
Labeler Code:
50536
Start Marketing Date: [9]
04-23-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 50536-103-10

Package Description: 10 SOLUTION in 1 POUCH

NDC Code 50536-103-20

Package Description: 20 SOLUTION in 1 POUCH

NDC Code 50536-103-25

Package Description: 250 SOLUTION in 1 PAIL

NDC Code 50536-103-30

Package Description: 30 SOLUTION in 1 POUCH

NDC Code 50536-103-60

Package Description: 60 SOLUTION in 1 POUCH

NDC Code 50536-103-80

Package Description: 80 SOLUTION in 1 POUCH

Product Details

What is NDC 50536-103?

The NDC code 50536-103 is assigned by the FDA to the product Alcohol Wipes which is product labeled by American Chemical And Sanitary Supply Inc. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 50536-103-10 10 solution in 1 pouch , 50536-103-20 20 solution in 1 pouch , 50536-103-25 250 solution in 1 pail , 50536-103-30 30 solution in 1 pouch , 50536-103-60 60 solution in 1 pouch , 50536-103-80 80 solution in 1 pouch . 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 Alcohol Wipes?

SUITABLE FOR CLEANSING AND HYGIENE FOR HOSPITAL MEDICAL STAFF AND NURSING STAFF, PUBLIC AREAS, HOUSEHOLD, PERSONAL CARE, AND SURFACES HYGIENE AND DISINFECTION DURING FLU SEASON.

Which are Alcohol Wipes UNII Codes?

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

Which are Alcohol Wipes 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:

* Please review the disclaimer below.

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".