NDC 0041-1420 Oral-b Anti-bacterial

  1. Labeler Index
  2. Oral-b Laboratories
  3. NDC: 0041-1420 Oral-b Anti-bacterial

NDC Product Code 0041-1420

NDC CODE: 0041-1420

Proprietary Name: Oral-b Anti-bacterial What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
MINT (C73404)

NDC Code Structure

  • 0041 - Oral-b Laboratories

NDC 0041-1420-16

Package Description: 500 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Oral-b Anti-bacterial with NDC 0041-1420 is a product labeled by Oral-b Laboratories. The generic name of Oral-b Anti-bacterial is . The product's dosage form is and is administered via form.

Labeler Name: Oral-b Laboratories

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Oral-b Laboratories
Labeler Code: 0041
Start Marketing Date: 10-15-2005 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Oral-b Anti-bacterial Product Label Images

Oral-b Anti-bacterial Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Cetylpyridinium Chloride 0.05%

Purpose

Anti-bacterial

Use

To fight plaque and bad breath bacteria.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.Not for use by children under six years of age.Children over six should be supervised when using this product.

Otc - Do Not Use

Do not use if shrinkband is broken or missing.

Otc - When Using

Do not swallow.

Directions

Rinse twice daily, after brushing, with 1/2 a capful (15 ml) for about 30 seconds.

Other Information

Store above freezing.

Inactive Ingredients

Water, Glycerin, Alcohol (9.3%), Flavor, Poloxamer 407, Methylparaben, Sodium Saccharin, Propylparaben, FD&C Blue #1, and D&C Yellow #10

Other

Distributed by: Oral-B, A Division of Procter & Gamble Cincinnati, OH 45202© Oral-B LaboratoriesMade in Colombia

* Please review the disclaimer below.