NDC 15304-4182 Mastic Dent Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 15304-4182?
What are the uses for Mastic Dent Whitening?
Which are Mastic Dent Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Mastic Dent Whitening 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:
- ENOXOLONE (UNII: P540XA09DR)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALLANTOIN (UNII: 344S277G0Z)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- MENTHOL (UNII: L7T10EIP3A)
- PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- .ALPHA.-BISABOLOL, ()- (UNII: 36HQN158VC)
- CHAMOMILE (UNII: FGL3685T2X)
What is the NDC to RxNorm Crosswalk for Mastic Dent Whitening?
- RxCUI: 245598 - sodium fluoride 0.22 % Toothpaste
- RxCUI: 245598 - sodium fluoride 0.0022 MG/MG Toothpaste
- RxCUI: 245598 - sodium fluoride 0.22 % (fluoride 0.1 % ) 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".