NDC 73297-001 Charcoal Mint Dentistry
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73297 - Jiangsu Shushi Biotechnology Co., Ltd.
- 73297-001 - Charcoal Mint Dentistry
Product Characteristics
Product Packages
NDC Code 73297-001-01
Package Description: 72 BOX in 1 CARTON / 1 TUBE in 1 BOX / 170.1 g in 1 TUBE
Product Details
What is NDC 73297-001?
What are the uses for Charcoal Mint Dentistry?
Which are Charcoal Mint Dentistry UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Charcoal Mint Dentistry 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:
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- WATER (UNII: 059QF0KO0R)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SACCHARIN (UNII: FST467XS7D)
- MENTHOL (UNII: L7T10EIP3A)
What is the NDC to RxNorm Crosswalk for Charcoal Mint Dentistry?
- RxCUI: 416783 - sodium fluoride 0.24 % Toothpaste
- RxCUI: 416783 - sodium fluoride 0.0024 MG/MG Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste
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[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".