NDC 71764-104 Oprecare 3set (07, 12, 21)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 71764-104?
What are the uses for Oprecare 3set (07, 12, 21)?
Which are Oprecare 3set (07, 12, 21) UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Oprecare 3set (07, 12, 21) 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- XYLITOL (UNII: VCQ006KQ1E)
- MENTHOL (UNII: L7T10EIP3A)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- UBIDECARENONE (UNII: EJ27X76M46)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STEVIOSIDE (UNII: 0YON5MXJ9P)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CHAMOMILE (UNII: FGL3685T2X)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- SALVIA OFFICINALIS ROOT (UNII: 236QY0A1BL)
- POMEGRANATE (UNII: 56687D1Z4D)
- ORANGE OIL (UNII: AKN3KSD11B)
- LICORICE (UNII: 61ZBX54883)
- ALLANTOIN (UNII: 344S277G0Z)
- PIRIDOCAINE HYDROCHLORIDE (UNII: VG6P406YHV)
- LEMON OIL (UNII: I9GRO824LL)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
What is the NDC to RxNorm Crosswalk for Oprecare 3set (07, 12, 21)?
- RxCUI: 1193319 - sodium monofluorophosphate 0.6 % Toothpaste
- RxCUI: 1193319 - sodium monofluorophosphate 0.006 MG/MG Toothpaste
* Please review the disclaimer below.
[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".