NDC 77935-401 Beanguard Sensitivetoothpaste
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 77935-401?
What are the uses for Beanguard Sensitivetoothpaste?
Which are Beanguard Sensitivetoothpaste UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- HYDRATED SILICA (UNII: Y6O7T4G8P9) (Active Moiety)
Which are Beanguard Sensitivetoothpaste 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- MARITIME PINE (UNII: 50JZ5Z98QY)
- STEVIOSIDE (UNII: 0YON5MXJ9P)
- MENTHOL (UNII: L7T10EIP3A)
- SOYBEAN (UNII: L7HT8F1ZOD)
- WATER (UNII: 059QF0KO0R)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- SORBITOL (UNII: 506T60A25R)
- EUCALYPTOL (UNII: RV6J6604TK)
- CHAMOMILE (UNII: FGL3685T2X)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- ROSEMARY (UNII: IJ67X351P9)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- BRASSICA OLERACEA WHOLE (UNII: FQ4E5MHM9Q)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
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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".