NDC 0041-1421 Oral-b Anticavity

  1. Labeler Index
  2. Oral-b Laboratories
  3. NDC: 0041-1421 Oral-b Anticavity

NDC Product Code 0041-1421

NDC CODE: 0041-1421

Proprietary Name: Oral-b Anticavity 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):
BLUE (C48333)
Flavor(s):
MINT (C73404)

NDC Code Structure

  • 0041 - Oral-b Laboratories

NDC 0041-1421-16

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 Anticavity with NDC 0041-1421 is a product labeled by Oral-b Laboratories. The generic name of Oral-b Anticavity 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".

* Please review the disclaimer below.

Information for Patients

Fluoride

Fluoride is pronounced as (floor' ide)

Why is fluoride medication prescribed?
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 usu...
[Read More]

* Please review the disclaimer below.

Oral-b Anticavity Product Label Images

Oral-b Anticavity 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

Sodium Fluoride 0.05%

Purpose

Anticavity

Use

Aids in the prevention of dental cavities.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

Otc - Do Not Use

Do not use if shrinkband is broken or missing.

Directions

  • Adults and children 6 years and older: use once a day after brushing your teeth with toothpaste.Vigorously swish 10ml (as indicated inside cap) of rinse between your teeth for 1 minute then spit out. Do not swallow.Do not eat or drink for 30 minutes after rinsing.Instruct children under 12 years of age in good rinsing habits to minimize swallowing.Supervise children as necessary until capable of using without supervision.Consult a dentist or physician for use by children under 6 years of age.

Other Information

Store above freezing.

Inactive Ingredients

Water, Glycerin, PEG 40 Hydrogenated Castor Oil, Flavor, Sodium Benzoate, Potassium Sorbate, Phosphoric Acid, Sodium Saccharin, FD&C Blue #1

* Please review the disclaimer below.