75916-4018 NDC - SNOWSKIN SUNSCREEN ()

Drug Information

Product NDC: 75916-4018

Proprietary Name: SnowSkin Sunscreen

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:1/5/2011

Package Information

No. Package Code Package Description Billing Unit
175916-4018-140 mL in 1 TUBE (75916-4018-1)
275916-4018-4125 mL in 1 TUBE (75916-4018-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75916-4018The 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 NAMESnowSkin 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 DATE1/5/2011This 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