NDC 74355-111 Unpaste Tooth Tabs

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:
74355-111
Proprietary Name:
Unpaste Tooth Tabs
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avespan Llc
Labeler Code:
74355
Start Marketing Date: [9]
05-15-2020
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 74355-111-01

Package Description: 125 BOX, UNIT-DOSE in 1 PACKET / 312 mg in 1 BOX, UNIT-DOSE

NDC Code 74355-111-10

Package Description: 10000 BOX, UNIT-DOSE in 1 CARTON / 312 mg in 1 BOX, UNIT-DOSE

Product Details

What is NDC 74355-111?

The NDC code 74355-111 is assigned by the FDA to the product Unpaste Tooth Tabs which is product labeled by Avespan Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74355-111-01 125 box, unit-dose in 1 packet / 312 mg in 1 box, unit-dose, 74355-111-10 10000 box, unit-dose in 1 carton / 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 Unpaste Tooth Tabs?

Adults and children 6 years of age and older; chew one tablet briefly and brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.Do not swallow the tablet.Supervise children under 6 years of age for brushing and rinsing.

Which are Unpaste Tooth Tabs UNII Codes?

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

Which are Unpaste Tooth Tabs 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:

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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".