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  4. NDC Product Code: 39892-0601 Medichoice Anticavity Fluoride

NDC 39892-0601 Medichoice Anticavity Fluoride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 39892-0601?
  4. Medichoice Anticavity Fluoride Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
39892-0601
Proprietary Name:
Medichoice Anticavity Fluoride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Owens And Minor
Labeler Code:
39892
Product Label ID:
306f908b-8cc3-4a79-9334-d8e9c4a86e11
Start Marketing Date: [9]
05-18-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 39892-0601?

The NDC code 39892-0601 is assigned by the FDA to the product Medichoice Anticavity Fluoride which is product labeled by Owens And Minor. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 39892-0601-1 5 box in 1 case / 144 tube in 1 box / 17 g in 1 tube, 39892-0601-2 5 box in 1 case / 144 tube in 1 box / 24 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 Medichoice Anticavity Fluoride?

Adults and children 2 yrs and older: Brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or physician.Children under 6 yrs: To minimize swallowing use a pea-sized amount and supervise brushing until good habits are established.Children under 2 years: Ask a dentist or physician.

Which are Medichoice Anticavity Fluoride UNII Codes?

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

Which are Medichoice Anticavity Fluoride 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 Medichoice Anticavity Fluoride?

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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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".