NDC 70926-100 Linhart

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:
70926-100
Proprietary Name:
Linhart
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Linhart Inc
Labeler Code:
70926
Start Marketing Date: [9]
08-17-2017
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404)

Product Packages

NDC Code 70926-100-34

Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE

NDC Code 70926-100-64

Package Description: 1 TUBE in 1 CARTON / 99 g in 1 TUBE

Product Details

What is NDC 70926-100?

The NDC code 70926-100 is assigned by the FDA to the product Linhart which is product labeled by Linhart Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70926-100-34 1 tube in 1 carton / 28 g in 1 tube, 70926-100-64 1 tube in 1 carton / 99 g in 1 tube. 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 Linhart?

Adults and Children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.Instruct children 6 years of age in good brushing and rinsing habits (to minimize swallowing), and and only use a pea size amount.Supervise children as necessary until capable of using without supervision.Chlidren under 2 years of age: Consult a dentist or doctor.

Which are Linhart UNII Codes?

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

Which are Linhart 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 Linhart?

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:

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Patient Education

Fluoride


Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".