NDC 51289-500 Toothpowder

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51289-500
Proprietary Name:
Toothpowder
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yangzhou Hengyuan Daily Chemical Plastic Co.,ltd
Labeler Code:
51289
Start Marketing Date: [9]
09-04-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 51289-500-01

Package Description: 250 BAG in 1 CARTON / 28 g in 1 BAG

NDC Code 51289-500-02

Package Description: 250 BAG in 1 CARTON / 57 g in 1 BAG

NDC Code 51289-500-03

Package Description: 250 BAG in 1 CARTON / 85 g in 1 BAG

Product Details

What is NDC 51289-500?

The NDC code 51289-500 is assigned by the FDA to the product Toothpowder which is product labeled by Yangzhou Hengyuan Daily Chemical Plastic Co.,ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 51289-500-01 250 bag in 1 carton / 28 g in 1 bag, 51289-500-02 250 bag in 1 carton / 57 g in 1 bag, 51289-500-03 250 bag in 1 carton / 85 g in 1 bag. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Toothpowder?

Adults and children 2years of age and older:Brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by a dentist or a physician.Children 2-6 years:Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)Children under 2 years:Ask a dentist or a physician.

Which are Toothpowder UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Toothpowder Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".