71035-400 NDC - FLUORIDE GEL ()

Drug Information

Product NDC: 71035-400

Proprietary Name: Fluoride Gel

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Yangzhou Hongshengding Chemical Co.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	5/1/2015

No.	Package Code	Package Description
1	71035-400-01	720 TUBE in 1 BOX (71035-400-01) / 17 g in 1 TUBE
2	71035-400-02	720 TUBE in 1 BOX (71035-400-02) / 24 g in 1 TUBE
3	71035-400-03	144 TUBE in 1 BOX (71035-400-03) / 43 g in 1 TUBE
4	71035-400-04	1000 TUBE in 1 BOX (71035-400-04) / .22 g in 1 TUBE
5	71035-400-05	1000 TUBE in 1 BOX (71035-400-05) / 7 g in 1 TUBE

Field Name	Field Value	Definition
PRODUCT NDC	71035-400	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	Fluoride Gel	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	5/1/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Yangzhou Hongshengding Chemical Co.,Ltd.	Name of Company corresponding to the labeler code segment of the Product NDC.

Export to text format icon Download this NDC record in Text format: Export

Export to text format icon Download this NDC record in Excel (CSV) format: Export

Export to text format icon Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023