71486-8036 NDC - GLINT ()

Drug Information

Product NDC: 71486-8036

Proprietary Name: Glint

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Glint Cosmetics Private Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/1/2014

Package Information

No. Package Code Package Description Billing Unit
171486-8036-2100 g in 1 TUBE (71486-8036-2)
271486-8036-3425 g in 1 JAR (71486-8036-3)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71486-8036The 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 NAMEGlintThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXVitamin A DA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE11/1/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGlint Cosmetics Private LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 9/11/2020