81569-010 NDC - D.S CRYSTAL TOOTH ()

Drug Information

Product NDC: 81569-010

Proprietary Name: D.S Crystal Tooth

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	81569-010-02	1 TUBE in 1 CARTON (81569-010-02) / 120 g in 1 TUBE (81569-010-01)

Field Name	Field Value	Definition
PRODUCT NDC	81569-010	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	D.S Crystal Tooth	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	2/1/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Taeyang Crystal	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