57913-2815 NDC - LUMINOUS INTENSIVE DECOLLOTE TREATMENT SPF 20 ()

Drug Information

Product NDC: 57913-2815

Proprietary Name: Luminous Intensive Decollote Treatment SPF 20

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Erno Laszlo, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/10/2013

Package Information

No. Package Code Package Description Billing Unit
157913-2815-01 JAR in 1 CARTON (57913-2815-0) / 50 mL in 1 JAR

NDC Record

Field Name Field Value Definition
PRODUCT NDC57913-2815The 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 NAMELuminous Intensive Decollote Treatment SPF 20The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/10/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEErno Laszlo, Inc.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