10481-0112 NDC - MONSELS SOLUTION ()

Drug Information

Product NDC: 10481-0112
Proprietary Name: MONSELS SOLUTION
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

Labeler Information

Field Name	Field Value
Labeler Name:	Gordon Laboratories
Product Type:
FDA Application Number:
Marketing Category:	UNAPPROVED DRUG OTHER
Start Marketing Date:	2/9/2010

Package Information

No.	Package Code	Package Description	Billing Unit
1	10481-0112-2	59 g in 1 BOTTLE, GLASS (10481-0112-2)	ML
2	10481-0112-8	8 g in 1 BOTTLE, GLASS (10481-0112-8)	ML

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	10481-0112	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	MONSELS SOLUTION	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	12/7/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Gordon Laboratories	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	10481-0112	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	MONSELS SOLUTION	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	2/9/2010	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Gordon Laboratories	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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