73029-0006 NDC - DR. ZENNI GUM PROJECT PROPOLI TOOTH FOR GUM DISEASE ()

Drug Information

Product NDC: 73029-0006

Proprietary Name: Dr. Zenni Gum Project Propoli Tooth for Gum Disease

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Zeniton Co.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2019

Package Information

No. Package Code Package Description Billing Unit
173029-0006-1100 g in 1 TUBE (73029-0006-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73029-0006The 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 NAMEDr. Zenni Gum Project Propoli Tooth for Gum DiseaseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/1/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZeniton Co.,Ltd.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