70781-004 NDC - BLANX ADVANCED WHITENING ()

Drug Information

Product NDC: 70781-004

Proprietary Name: BlanX Advanced Whitening

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Coswell Spa
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/26/2017

Package Information

No. Package Code Package Description Billing Unit
170781-004-0175 g in 1 TUBE (70781-004-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70781-004The 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 NAMEBlanX Advanced WhiteningThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/26/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECoswell SpaName 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