NDC 63956-001 Emmi Dent Sodium Fluoride Anticavity Mild
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63956-001?
What are the uses for Emmi Dent Sodium Fluoride Anticavity Mild?
Which are Emmi Dent Sodium Fluoride Anticavity Mild 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 Emmi Dent Sodium Fluoride Anticavity Mild 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)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SORBITOL (UNII: 506T60A25R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POTASSIUM PYROPHOSPHATE (UNII: B9W4019H5G)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- ALLANTOIN (UNII: 344S277G0Z)
- LIMONEN-10-OL, (+)- (UNII: 1Q8KVB0R3J)
- CHAMOMILE (UNII: FGL3685T2X)
- THREE-LOBE SAGE (UNII: 3V97D33N0K)
- CITRAL (UNII: T7EU0O9VPP)
What is the NDC to RxNorm Crosswalk for Emmi Dent Sodium Fluoride Anticavity Mild?
- RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
- RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (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".