NDC 69152-0119 Glowin 40 (number 119)

Product Information

What is NDC 69152-0119?

The NDC code 69152-0119 is assigned by the FDA to the product Glowin 40 (number 119) which is product labeled by Paramesh Banerji Life Sciences Llc. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 69152-0119-1 96 pellet 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, RxNorm crosswalk and the complete product label.

NDC Product Code69152-0119
Proprietary Name 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.		Glowin 40 (number 119)
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Paramesh Banerji Life Sciences Llc
Labeler Code69152
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		10-29-2014
Listing Expiration Date 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.		12-31-2019
Exclude Flag 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". 		I
NDC Code Structure

What are the uses for Glowin 40 (number 119)?


Product Characteristics

Color(s)WHITE (C48325)
ShapeROUND (C48348)
Size(s)4 MM

Product Packages

NDC Code 69152-0119-1

Package Description: 96 PELLET in 1 BOTTLE

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

Product Details

Glowin 40 (number 119) Active Ingredients UNII Codes

Glowin 40 (number 119) 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.

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Glowin 40 (number 119) Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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