NDC 53943-557 Discount Drug Mart Blue Mint Mouthwash
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53943-557?
What are the uses for Discount Drug Mart Blue Mint Mouthwash?
Which are Discount Drug Mart Blue Mint Mouthwash 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)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- THYMOL (UNII: 3J50XA376E)
- THYMOL (UNII: 3J50XA376E) (Active Moiety)
Which are Discount Drug Mart Blue Mint Mouthwash 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)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
What is the NDC to RxNorm Crosswalk for Discount Drug Mart Blue Mint Mouthwash?
- 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".