62032-526 NDC - OBAGI MEDICAL - NU-DERM SYSTEM - NORMAL TO DRY - SKIN TRANSFORMATION KIT ()

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Drug Information

Product NDC: 62032-526

Proprietary Name: Obagi Medical - Nu-Derm System - Normal to Dry - Skin Transformation Kit

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name:	OMP, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	12/10/2015

Package Information

No.	Package Code	Package Description	Billing Unit
1	62032-526-06	1 KIT in 1 CARTON (62032-526-06) * 57 g in 1 TUBE * 57 g in 1 TUBE * 85 g in 1 TUBE

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	62032-526	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	Obagi Medical - Nu-Derm System - Normal to Dry - Skin Transformation Kit	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	12/10/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	OMP, Inc.	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

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