NDC 15304-4085 Mastic Dent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 15304 - Chia Gi Ltd
- 15304-4085 - Mastic Dent
Product Characteristics
Product Packages
NDC Code 15304-4085-1
Package Description: 400 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 15304-4085?
What are the uses for Mastic Dent?
Which are Mastic Dent UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- EUCALYPTOL (UNII: RV6J6604TK)
- EUCALYPTOL (UNII: RV6J6604TK) (Active Moiety)
- THYMOL (UNII: 3J50XA376E)
- THYMOL (UNII: 3J50XA376E) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Mastic Dent 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:
- SORBITOL (UNII: 506T60A25R)
- PISTACIA LENTISCUS SEED OIL (UNII: Z7D029774C)
- PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALCOHOL (UNII: 3K9958V90M)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Mastic Dent?
- RxCUI: 1363759 - eucalyptol 0.092 % / menthol 0.042 % / sodium fluoride 0.025 % / thymol 0.064 % Mouthwash
- RxCUI: 1363759 - eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / sodium fluoride 0.25 MG/ML / thymol 0.64 MG/ML Mouthwash
* 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".