NDC 68983-006 Ibrite
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 68983-006?
Which are Ibrite UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
Which are Ibrite 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:
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM PHOSPHATE, TRIBASIC (UNII: A752Q30A6X)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
What is the NDC to RxNorm Crosswalk for Ibrite?
- RxCUI: 1734689 - potassium nitrate 3 % / sodium fluoride 0.254 % Toothpaste
- RxCUI: 1734689 - potassium nitrate 0.03 MG/MG / sodium fluoride 0.00254 MG/MG Toothpaste
- RxCUI: 1734689 - K+ nitrate 0.03 MG/MG / Sodium Fluoride 0.00254 MG/MG Toothpaste
- RxCUI: 1734689 - Pot nitrate 0.03 MG/MG / Sodium Fluoride 0.00254 MG/MG 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".