NDC 61543-7233 Plus White With Peroxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61543 - Cca Industries, Inc.
- 61543-7233 - Plus White With Peroxide
Product Packages
NDC Code 61543-7233-2
Package Description: 1 TUBE in 1 BOX / 100 g in 1 TUBE
Product Details
What is NDC 61543-7233?
What are the uses for Plus White With Peroxide?
Which are Plus White With Peroxide UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
Which are Plus White With Peroxide 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- SORBITOL (UNII: 506T60A25R)
- UREA (UNII: 8W8T17847W)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- CALCIUM PEROXIDE (UNII: 7FRO2ENO91)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Plus White With Peroxide?
- RxCUI: 891795 - sodium monofluorophosphate 0.884 % Toothpaste
- RxCUI: 891795 - sodium monofluorophosphate 0.00884 MG/MG Toothpaste
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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".