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  4. NDC Product Code: 49741-1005 Medactive Patient Friendly

NDC 49741-1005 Medactive Patient Friendly

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49741-1005?
  5. Medactive Patient Friendly Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49741-1005
Proprietary Name:
Medactive Patient Friendly
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Integrate Oral Care, Llc.
Labeler Code:
49741
Product Label ID:
18bcb094-6257-4d1d-e054-00144ff88e88
Start Marketing Date: [9]
07-31-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
ORANGE (C73406 - ORANGE CRÈME WITH ULTRAMULSION® AND SPILANTHES EXTRACT)

Code Structure Chart

Product Details

What is NDC 49741-1005?

The NDC code 49741-1005 is assigned by the FDA to the product Medactive Patient Friendly which is product labeled by Integrate Oral Care, Llc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 49741-1005-2 10 carton in 1 box / 1 kit in 1 carton (49741-1005-1) * 3.7 ml in 1 kit * 27 ml in 1 kit, 49741-1005-3 30 carton in 1 box / 1 kit in 1 carton * 3.7 ml in 1 kit * 27 ml in 1 kit. 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 Medactive Patient Friendly?

UsesAids in the prevention of dental decay.

Which are Medactive Patient Friendly UNII Codes?

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

Which are Medactive Patient Friendly 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 Medactive Patient Friendly?

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:

* Please review the disclaimer below.

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".