62802-039 NDC - OP PROTECTIVE GEL 15 ()

Drug Information

Product NDC: 62802-039

Proprietary Name: OP Protective Gel 15

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sun & Skin Care Research, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2012

Package Information

No. Package Code Package Description Billing Unit
162802-039-85251 g in 1 BOTTLE (62802-039-85)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62802-039The 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 NAMEOP Protective Gel 15The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESun & Skin Care Research, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/18/2019