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  4. NDC Product Code: 86157-0014 Denti Whoo Blue Tabletgargle

NDC 86157-0014 Denti Whoo Blue Tabletgargle

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 86157-0014?
  5. Denti Whoo Blue Tabletgargle Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
86157-0014
Proprietary Name:
Denti Whoo Blue Tabletgargle
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sun Life Science Co Ltd
Labeler Code:
86157
Product Label ID:
df330e62-e8cd-7b1f-e053-2a95a90ac0ba
Start Marketing Date: [9]
04-06-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
15 MM
Imprint(s):
NONE
Score:
1
Flavor(s):
MENTHOL (C73403)

Product Packages

NDC Code 86157-0014-1

Package Description: 8 TABLET in 1 PACKAGE

Product Details

What is NDC 86157-0014?

The NDC code 86157-0014 is assigned by the FDA to the product Denti Whoo Blue Tabletgargle which is product labeled by Sun Life Science Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 86157-0014-1 8 tablet in 1 package . 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 Denti Whoo Blue Tabletgargle?

USAGE : Put 1 tablet in the mouth and use the tongue and lips to rub the gums, teeth, and tongue, gargle it with water, and rinse it several times

Which are Denti Whoo Blue Tabletgargle UNII Codes?

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

Which are Denti Whoo Blue Tabletgargle 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:

* 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".