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  4. NDC Product Code: 69491-220 Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope

NDC 69491-220 Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69491-220?
  5. Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69491-220
Proprietary Name:
Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Buzz Export Services Pty Ltd
Labeler Code:
69491
Product Label ID:
fa870de7-9cfd-43e0-86d4-1b7d532d4843
Start Marketing Date: [9]
07-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
PEPPERMINT (C73408)

Code Structure Chart

Product Details

What is NDC 69491-220?

The NDC code 69491-220 is assigned by the FDA to the product Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope which is product labeled by Buzz Export Services Pty Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69491-220-00 1 kit in 1 kit * 24 g in 1 tube (37000-020-01). 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 Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope?

Adults and children 2 yrs. & older: brush teeth thoroughly after meals of at least twice a day or use as directed by a dentistdo not swallowto minimize swallowing use a pea-sized amount in children under 6 supervise children's brushing until good habits are establishedchildren under 2 yrs.: ask a dentist

Which are Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope UNII Codes?

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

Which are Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope 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 Delta One 2019 Tumi Collins Amenity With Crest Complete Whitening Scope?

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: 891775 - sodium fluoride 0.243 % Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste

* 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".