70242-128 NDC - TINTUTA DE MENTIOLATE/MENTHIOLATE TINCTURE ()

Drug Information

Product NDC: 70242-128

Proprietary Name: Tintuta de Mentiolate/Menthiolate Tincture

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Dannso Corp./d.b.a. Essential Products
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	1/1/2015

No.	Package Code	Package Description	Billing Unit
1	70242-128-01	30 mL in 1 BOTTLE, PLASTIC (70242-128-01)

Field Name	Field Value	Definition
PRODUCT NDC	70242-128	The 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 NAME	Tintuta de Mentiolate/Menthiolate Tincture	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	1/1/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Dannso Corp./d.b.a. Essential Products	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