NDC 62111-0212 Professional Whitening System Whitening Mouth Wash

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62111-0212
Proprietary Name:
Professional Whitening System Whitening Mouth Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Akg Innovations Llc
Labeler Code:
62111
Start Marketing Date: [9]
02-14-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62111-0212-4

Package Description: 220 mL in 1 BOTTLE

Product Details

What is NDC 62111-0212?

The NDC code 62111-0212 is assigned by the FDA to the product Professional Whitening System Whitening Mouth Wash which is product labeled by Akg Innovations Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62111-0212-4 220 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Professional Whitening System Whitening Mouth Wash?

 Adults and children 12 years ofage or older:• use twice daily after brushing yourteeth with a toothpaste• vigorously swish 10 ml (2 teaspoonfuls)of rinse between your teeth for 1 minuteand then spit out• do not swallow the rinse• do not eat or drink for 30 minutesafter rinsing• supervise children as necessary untilcapable of using without supervision• Children under 12 years of age consulta dentist or doctor

Which are Professional Whitening System Whitening Mouth Wash UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Professional Whitening System Whitening Mouth Wash?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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.

Product Footnotes

[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".