NDC 62864-665 Truly Radiant Whitening And Strengthening Rinse Clean And Fresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62864 - Church & Dwight Canada Corp
- 62864-665 - Truly Radiant
Product Characteristics
Product Packages
NDC Code 62864-665-08
Package Description: 237 mL in 1 BOTTLE
NDC Code 62864-665-16
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 62864-665?
What are the uses for Truly Radiant Whitening And Strengthening Rinse Clean And Fresh?
Which are Truly Radiant Whitening And Strengthening Rinse Clean And Fresh 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 Truly Radiant Whitening And Strengthening Rinse Clean And Fresh 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:
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- XYLITOL (UNII: VCQ006KQ1E)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
What is the NDC to RxNorm Crosswalk for Truly Radiant Whitening And Strengthening Rinse Clean And Fresh?
- RxCUI: 313029 - sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse
- RxCUI: 313029 - sodium fluoride 0.2 MG/ML Mouthwash
- RxCUI: 313029 - sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral Rinse
* 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".