NDC 51289-500 Toothpowder

NDC Product Code 51289-500

NDC CODE: 51289-500

Proprietary Name: Toothpowder What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 51289-500-01

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

NDC 51289-500-02

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

NDC 51289-500-03

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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Toothpowder with NDC 51289-500 is a product labeled by Yangzhou Hengyuan Daily Chemical Plastic Co.,ltd. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Product Labeler Information

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

Labeler Name: Yangzhou Hengyuan Daily Chemical Plastic Co.,ltd
Labeler Code: 51289
Start Marketing Date: 09-04-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Toothpowder Product Label Images

Toothpowder Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Sodium Fluoride 0.24%(0.1 w/v Fluoride ion)




Helps protect against cavities.


Keep out of the reach of children under 6 years of age.if more than used for brushing is accidently swallowed,get medical help or contact a Poison Control Center immediately.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.


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.

Inactive Ingredient

Calcium carbonate,silica,mint falvour,sodium laryl sulfate ,sodium benzoate

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