62032-527 NDC - OBAGI NU-DERM FX SYSTEM - NORMAL TO DRY ()

Drug Information

Product NDC: 62032-527

Proprietary Name: Obagi Nu-Derm FX System - Normal to Dry

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:11/4/2015

Package Information

No. Package Code Package Description Billing Unit
162032-527-071 KIT in 1 CARTON (62032-527-07) * 85 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC62032-527The 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 NAMEObagi Nu-Derm FX System - Normal to DryThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/4/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOMP, 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