NDC 50241-246 Hand Sanitizer Solution 101

  1. Labeler Index
  2. Morgan Gallacher Inc. Dba Custom Chemical Formulators Inc.
  3. NDC: 50241-246 Hand Sanitizer Solution 101

NDC Product Code 50241-246

NDC CODE: 50241-246

Proprietary Name: Hand Sanitizer Solution 101 What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 50241 - Morgan Gallacher Inc. Dba Custom Chemical Formulators Inc.

NDC 50241-246-01

Package Description: 4 DRUM in 1 BOX > 202.07 kg in 1 DRUM (50241-246-08)

NDC 50241-246-02

Package Description: 3.67 kg in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Hand Sanitizer Solution 101 with NDC 50241-246 is a product labeled by Morgan Gallacher Inc. Dba Custom Chemical Formulators Inc.. The generic name of Hand Sanitizer Solution 101 is . The product's dosage form is and is administered via form.

Labeler Name: Morgan Gallacher Inc. Dba Custom Chemical Formulators Inc.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Morgan Gallacher Inc. Dba Custom Chemical Formulators Inc.
Labeler Code: 50241
Start Marketing Date: 11-13-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Hand Sanitizer Solution 101 Product Label Images

Hand Sanitizer Solution 101 Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Benzalkoium Chloride.....0.13%

Purpose

Antimicrobial

Uses

For Hand Sanitizing to decrease bacteria on the skin

Warnings:

- For external use only-Flammable keep away from fire or flame​
​When using this product-Avoid contact with the eyesIn case of eye contact, flush eyes with water.

Directions

-Wash hands with soap and water Rinse with potable water- wet entire surface of hands with product especially the cuticles and fingernails -Rub hands together until dry - Do not rinse hands - Re-apply as needed

Inactive Ingredients

Isopropyl Alcohol, Water

* Please review the disclaimer below.