62032-908 NDC - OBAGI SKINTRINSIQ ANTIOXIDANT PROTOCOL ()

Drug Information

Product NDC: 62032-908

Proprietary Name: Obagi Skintrinsiq Antioxidant Protocol

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Obagi Cosmeceuticals LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/1/2021

Package Information

No. Package Code Package Description Billing Unit
162032-908-081 KIT in 1 BOX (62032-908-08) * 1 BOTTLE, DROPPER in 1 CARTON / 30 mL in 1 BOTTLE, DROPPER * 1 BOTTLE, PUMP in 1 CARTON / 30 mL in 1 BOTTLE, PUMP * 1 BOTTLE, PUMP in 1 CARTON / 48 g in 1 BOTTLE, PUMP * 59 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC62032-908The 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 Skintrinsiq Antioxidant ProtocolThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEObagi Cosmeceuticals LLCName 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