NDC 57367-033 Therabreath Toothpaste
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 57367-033?
What are the uses for Therabreath Toothpaste?
Which are Therabreath Toothpaste 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 Therabreath Toothpaste 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:
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CHLORITE (UNII: G538EBV4VF)
- ALOE (UNII: V5VD430YW9)
What is the NDC to RxNorm Crosswalk for Therabreath Toothpaste?
- 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".