NDC 62111-0213 Professional Whitening System Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62111 - Akg Innovations Llc
- 62111-0213 - Professional Whitening System Whitening
Product Packages
NDC Code 62111-0213-2
Package Description: 1 TUBE in 1 PACKAGE / 113.6 g in 1 TUBE
Product Details
What is NDC 62111-0213?
What are the uses for Professional Whitening System Whitening?
Which are Professional Whitening System Whitening 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 Professional Whitening System Whitening 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:
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- GLYCERIN (UNII: PDC6A3C0OX)
- XYLITOL (UNII: VCQ006KQ1E)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- SODIUM SARCOSINATE (UNII: 6EHN3PQL8Z)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- MENTHOL (UNII: L7T10EIP3A)
- SALVADORA PERSICA ROOT (UNII: 526M7ZU616)
What is the NDC to RxNorm Crosswalk for Professional Whitening System Whitening?
- RxCUI: 1489127 - sodium fluoride 0.23 % Toothpaste
- RxCUI: 1489127 - sodium fluoride 0.0023 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".