NDC 79763-008 Vvardis Set Strong Mint
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 79763-008?
What are the uses for Vvardis Set Strong Mint?
Which are Vvardis Set Strong Mint UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
Which are Vvardis Set Strong Mint 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:
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ZINC LACTATE (UNII: 2GXR25858Y)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM COCO-SULFATE (UNII: 3599J29ANH)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- RHODODENDRON FERRUGINEUM WHOLE (UNII: FO6B1S7BZU)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL (UNII: 506T60A25R)
- LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
What is the NDC to RxNorm Crosswalk for Vvardis Set Strong Mint?
- RxCUI: 1546238 - sodium monofluorophosphate 0.88 % Toothpaste
- RxCUI: 1546238 - sodium monofluorophosphate 0.0088 MG/MG Toothpaste
- RxCUI: 1546238 - sodium monofluorophosphate 0.88 % (fluoride ion 0.115 % )Toothpaste
- 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.
[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".