NDC 82756-002 Tidalove Smile More Oral Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
CINNAMON (C73377)
Code Structure Chart
Product Details
What is NDC 82756-002?
What are the uses for Tidalove Smile More Oral Care?
Which are Tidalove Smile More Oral 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 Tidalove Smile More Oral 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:
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SORBITOL (UNII: 506T60A25R)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- XYLITOL (UNII: VCQ006KQ1E)
- ROSEMARY (UNII: IJ67X351P9)
- SEA SALT (UNII: 87GE52P74G)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM ASCORBATE (UNII: S033EH8359)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
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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".