NDC 62111-0212 Professional Whitening System Whitening Mouth Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62111 - Akg Innovations Llc
- 62111-0212 - Professional Whitening System Whitening Mouth Wash
Product Packages
NDC Code 62111-0212-4
Package Description: 220 mL in 1 BOTTLE
Product Details
What is NDC 62111-0212?
What are the uses for Professional Whitening System Whitening Mouth Wash?
Which are Professional Whitening System Whitening Mouth Wash 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 Mouth Wash 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)
- XYLITOL (UNII: VCQ006KQ1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- CASTOR OIL (UNII: D5340Y2I9G)
- MENTHOL (UNII: L7T10EIP3A)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SALVADORA PERSICA ROOT (UNII: 526M7ZU616)
- ZINC LACTATE (UNII: 2GXR25858Y)
What is the NDC to RxNorm Crosswalk for Professional Whitening System Whitening Mouth Wash?
- 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
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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".