71153-2000 NDC - GP SUNSCREEN ()

Drug Information

Product NDC: 71153-2000

Proprietary Name: gp sunscreen

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Cross-Brands Manufacturing, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/23/2016

Package Information

No. Package Code Package Description Billing Unit
171153-2000-1237 mL in 1 BOTTLE (71153-2000-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71153-2000The 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 NAMEgp sunscreenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/23/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECross-Brands Manufacturing, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/3/2024