58411-238 NDC - SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER ()

Drug Information

Product NDC: 58411-238

Proprietary Name: SHISEIDO WHITE LUCENT ALL DAY BRIGHTENER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: SHISEIDO AMERICAS CORPORATION
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2015

Package Information

No. Package Code Package Description Billing Unit
158411-238-601 TUBE in 1 CARTON (58411-238-60) > 50 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC58411-238The 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 NAMESHISEIDO WHITE LUCENT ALL DAY BRIGHTENERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/1/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESHISEIDO AMERICAS CORPORATIONName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/3/2020