75916-0636 NDC - SURFERSSKIN SUNSCREEN ZINC ()

Drug Information

Product NDC: 75916-0636

Proprietary Name: SurfersSkin Sunscreen Zinc

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Skin Alive, Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/27/2011

Package Information

No. Package Code Package Description Billing Unit
175916-0636-11 TUBE, WITH APPLICATOR in 1 BOX (75916-0636-1) / 8.5 g in 1 TUBE, WITH APPLICATOR

NDC Record

Field Name Field Value Definition
PRODUCT NDC75916-0636The 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 NAMESurfersSkin Sunscreen ZincThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/27/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESkin Alive, Ltd.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