NDC 77982-114 X-pur Opti-rinse Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77982 - Laboratoires Msp Inc
- 77982-114 - X-pur Opti-rinse Plus
Product Packages
NDC Code 77982-114-11
Package Description: 500 mL in 1 BOTTLE
Product Details
What is NDC 77982-114?
What are the uses for X-pur Opti-rinse Plus?
Which are X-pur Opti-rinse Plus 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 X-pur Opti-rinse Plus 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- XYLITOL (UNII: VCQ006KQ1E)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- MINT (UNII: FV98Z8GITP)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
- WATER (UNII: 059QF0KO0R)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
What is the NDC to RxNorm Crosswalk for X-pur Opti-rinse Plus?
- RxCUI: 240698 - sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
- RxCUI: 240698 - sodium fluoride 0.5 MG/ML Mouthwash
* Please review the disclaimer below.
Patient Education
Fluoride
Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".