NDC 63404-1984 Sprinjene Natural Sensitivity And Gum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63404 - Health And Natural Beauty Usa Corp
- 63404-1984 - Sprinjene Natural
Product Characteristics
Product Packages
NDC Code 63404-1984-1
Package Description: 1 TUBE in 1 CARTON / 142 g in 1 TUBE
Product Details
What is NDC 63404-1984?
What are the uses for Sprinjene Natural Sensitivity And Gum?
Which are Sprinjene Natural Sensitivity And Gum 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 Sprinjene Natural Sensitivity And Gum 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)
- XYLITOL (UNII: VCQ006KQ1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPANEDIOL (UNII: 5965N8W85T)
- ZINC CITRATE (UNII: K72I3DEX9B)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- NIGELLA SATIVA SEED OIL (UNII: CS4U38E731)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- STEVIA SERRATA FLOWER OIL (UNII: 93Z447IP63)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ACACIA (UNII: 5C5403N26O)
- POMEGRANATE (UNII: 56687D1Z4D)
- THYME OIL (UNII: 2UK410MY6B)
- TEA TREE OIL (UNII: VIF565UC2G)
What is the NDC to RxNorm Crosswalk for Sprinjene Natural Sensitivity And Gum?
- 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
* Please review the disclaimer below.
[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".