NDC 80487-111 Kindfill

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:
80487-111
Proprietary Name:
Kindfill
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
By Humankind Inc
Labeler Code:
80487
Start Marketing Date: [9]
10-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
NONE
Score:
1
Flavor(s):
PEPPERMINT (C73408)

Product Packages

NDC Code 80487-111-11

Package Description: 60 BOX, UNIT-DOSE in 1 BOX / 312 mg in 1 BOX, UNIT-DOSE

Product Details

What is NDC 80487-111?

The NDC code 80487-111 is assigned by the FDA to the product Kindfill which is product labeled by By Humankind Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80487-111-11 60 box, unit-dose in 1 box / 312 mg in 1 box, unit-dose. 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 Kindfill?

Adults and children 6 years of age and older; chew one tablet until crushed, wet toothbrush, brush for 2 minutes. Spit out.Do not swallow the tablet.Children under 6 years of age should be supervised when using this product.

Which are Kindfill UNII Codes?

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

Which are Kindfill 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".