NDC 11822-3705 Anticavity Fluoride Rinse
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-3705 - Anticavity Fluoride Rinse
Product Packages
NDC Code 11822-3705-4
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11822-3705?
What are the uses for Anticavity Fluoride Rinse?
Which are Anticavity Fluoride Rinse 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 Anticavity Fluoride 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)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- EUCALYPTOL (UNII: RV6J6604TK)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- THYMOL (UNII: 3J50XA376E)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- MENTHOL (UNII: L7T10EIP3A)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Anticavity Fluoride Rinse?
- RxCUI: 1038904 - sodium fluoride 0.0221 % (fluoride ion 0.01 % ) Mouthwash
- RxCUI: 1038904 - sodium fluoride 0.221 MG/ML Mouthwash
- RxCUI: 1038904 - sodium fluoride 0.0221 % (fluoride 0.01 % ) Oral Rinse
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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".