NDC 61995-1562 Jason Total Protection Sensitive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 61995-1562?
What are the uses for Jason Total Protection Sensitive?
Which are Jason Total Protection Sensitive UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
Which are Jason Total Protection Sensitive 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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- PEPPERMINT (UNII: V95R5KMY2B)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- CURCUMA LONGA WHOLE (UNII: W5488JUO8U)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- ETLINGERA ELATIOR WHOLE (UNII: KF7S33DH97)
- CLOVE OIL (UNII: 578389D6D0)
What is the NDC to RxNorm Crosswalk for Jason Total Protection Sensitive?
- RxCUI: 312544 - potassium nitrate 5 % Toothpaste
- RxCUI: 312544 - potassium nitrate 0.05 MG/MG Toothpaste
- RxCUI: 312544 - K+ nitrate 0.05 MG/MG Toothpaste
- RxCUI: 312544 - Pot nitrate 0.05 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".