59151-646 NDC - SKIN AND SCALP BODY ()

Drug Information

Product NDC: 59151-646

Proprietary Name: Skin and Scalp Body

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Albra Dewyn LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/1/2016

Package Information

No. Package Code Package Description Billing Unit
159151-646-04118 mL in 1 BOTTLE (59151-646-04)
259151-646-08237 mL in 1 BOTTLE (59151-646-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59151-646The 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 NAMESkin and Scalp BodyThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/3/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAlbra Dewyn LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC59151-646The 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 NAMESkin and Scalp BodyThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAlbra Dewyn LLCName 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