NDC 70766-005 Amerfresh Tooth

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:
70766-005
Proprietary Name:
Amerfresh Tooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70766
Start Marketing Date: [9]
04-20-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 70766-005?

The NDC code 70766-005 is assigned by the FDA to the product Amerfresh Tooth which is product labeled by Yangzhou Sion Commodity Co.,ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70766-005-01 40 package in 1 carton / 454 g in 1 package, 70766-005-02 4 box in 1 carton / 50 pouch in 1 box / 57 g in 1 pouch. 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 Amerfresh Tooth?

For Use:Wet toothbrush and dip into powder until brush is fully covereddo not swallow .supervise children as necessary until capable of useing without supervisioninstruct children under 12 years of age in good brushing and rinsing habits(to minimize swallowing).Adults and children 6 years 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 under 6 years of age:do not use unless directed by a doctor or dentist.

Which are Amerfresh Tooth UNII Codes?

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

Which are Amerfresh Tooth 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:

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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".