NDC 83812-003 Glorysmile Toothpaste.
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 83812-003?
What are the uses for Glorysmile Toothpaste.?
Which are Glorysmile Toothpaste. UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
Which are Glorysmile Toothpaste. 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:
- XANTHAN GUM (UNII: TTV12P4NEE)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- ZINC LACTATE (UNII: 2GXR25858Y)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- CALCIUM GLYCEROPHOSPHATE (UNII: XWV9Z12C1C)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- SORBITOL (UNII: 506T60A25R)
- XYLITOL (UNII: VCQ006KQ1E)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- POTASSIUM PYROPHOSPHATE (UNII: B9W4019H5G)
- MENTHOL (UNII: L7T10EIP3A)
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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".