72362-101 NDC - MOISTU-EYES ()

Drug Information

Product NDC: 72362-101

Proprietary Name: MOISTU-EYES

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	BRASSICA PHARMA PRIVATE LIMITED
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	6/11/2018

No.	Package Code	Package Description	Billing Unit
1	72362-101-01	1 TUBE in 1 CARTON (72362-101-01) / 3.5 g in 1 TUBE
2	72362-101-02	1 TUBE in 1 CARTON (72362-101-02) / 5 g in 1 TUBE

Field Name	Field Value	Definition
PRODUCT NDC	72362-101	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	MOISTU-EYES	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	6/11/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	BRASSICA PHARMA PRIVATE LIMITED	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023