42851-031 NDC - MELAMIX SKIN LIGHTENER AND BLENDING ()

Drug Information

Product NDC: 42851-031

Proprietary Name: MELAMIX Skin Lightener and Blending

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ZO Skin Health, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2012

Package Information

No. Package Code Package Description Billing Unit
142851-031-321 BOTTLE, PLASTIC in 1 CARTON (42851-031-32) / 32 g in 1 BOTTLE, PLASTIC
242851-031-801 BOTTLE, PLASTIC in 1 CARTON (42851-031-80) / 80 g in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC42851-031The 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 NAMEMELAMIX Skin Lightener and BlendingThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZO Skin Health, 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