NDC 61995-0104 Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint
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What is NDC 61995-0104?
What are the uses for Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint?
Which are Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- MONOFLUOROPHOSPHATE ION (UNII: 4964UZ79MI) (Active Moiety)
Which are Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- XYLITOL (UNII: VCQ006KQ1E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BAMBUSA ARUNDINACEA STEM (UNII: NRA4497HC5)
- CITRUS MAXIMA SEED (UNII: 083X55C543)
- PARSLEY (UNII: 58FMD0Q0EV)
- PERILLA FRUTESCENS SEED (UNII: 8M62PUD356)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- SPEARMINT OIL (UNII: C3M81465G5)
- APHANIZOMENON FLOS-AQUAE (UNII: 49VG1X560X)
- UBIDECARENONE (UNII: EJ27X76M46)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- SEA SALT (UNII: 87GE52P74G)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Jason Sea Fresh Anticavity Strengthening Deep Sea Spearmint?
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste
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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".