NDC 72382-001 Dr Plus Dental Daily Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 72382-001?
What are the uses for Dr Plus Dental Daily Care?
Which are Dr Plus Dental Daily Care 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 Dr Plus Dental Daily Care 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:
- XYLITOL (UNII: VCQ006KQ1E)
- SORBITOL (UNII: 506T60A25R)
- MALIC ACID (UNII: 817L1N4CKP)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- LYSINE (UNII: K3Z4F929H6)
- ARGININE (UNII: 94ZLA3W45F)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PLATYCODON GRANDIFLORUS ROOT (UNII: 2DF0NS0O2Z)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- GARDENIA JASMINOIDES WHOLE (UNII: 0PK353KHF0)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- VITIS VINIFERA ANTHOCYANINS (UNII: F02KPB2508)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
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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".