NDC 36800-210 Antiseptic Mouth Rinse
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 36800-210?
What are the uses for Antiseptic Mouth Rinse?
Which are Antiseptic Mouth Rinse UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUCALYPTOL (UNII: RV6J6604TK)
- EUCALYPTOL (UNII: RV6J6604TK) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- THYMOL (UNII: 3J50XA376E)
- THYMOL (UNII: 3J50XA376E) (Active Moiety)
Which are Antiseptic Mouth Rinse 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- SORBITOL (UNII: 506T60A25R)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Antiseptic Mouth Rinse?
- RxCUI: 1043619 - eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash
- RxCUI: 1043619 - eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / methyl salicylate 0.6 MG/ML / thymol 0.64 MG/ML Mouthwash
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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".