NDC 53943-554 Discount Drug Mart Anticavity Fluoride Rinse Mint Flavor
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 53943-554?
What are the uses for Discount Drug Mart Anticavity Fluoride Rinse Mint Flavor?
Which are Discount Drug Mart Anticavity Fluoride Rinse Mint Flavor 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 Discount Drug Mart Anticavity Fluoride Rinse Mint Flavor 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:
- EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- MENTHOL (UNII: L7T10EIP3A)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Discount Drug Mart Anticavity Fluoride Rinse Mint Flavor?
- RxCUI: 240698 - sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
- RxCUI: 240698 - sodium fluoride 0.5 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".