NDC 55754-122 Zohar Toothpaste Cool Mint
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55754 - Broom Lane Enterprises
- 55754-122 - Zohar Toothpaste
Product Packages
NDC Code 55754-122-01
Package Description: 1 TUBE in 1 CARTON / 113.4 g in 1 TUBE
Product Details
What is NDC 55754-122?
What are the uses for Zohar Toothpaste Cool Mint?
Which are Zohar Toothpaste Cool Mint UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Zohar Toothpaste Cool Mint 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)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CARVONE, (+/-)- (UNII: 75GK9XIA8I)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- METHYLPARABEN (UNII: A2I8C7HI9T)
What is the NDC to RxNorm Crosswalk for Zohar Toothpaste Cool Mint?
- RxCUI: 1045495 - sodium monofluorophosphate 1.15 % Toothpaste
- RxCUI: 1045495 - sodium monofluorophosphate 0.0115 MG/MG Toothpaste
- RxCUI: 1045495 - sodium monofluorophosphate 1.15 % (0.15 % w/v fluoride ion) 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".