Oral-b
FDA Label NDC 0041-1420

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Oral-b Laboratories for the product Oral-b (NDC 0041-1420). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, otc - keep out of reach of children, otc - do not use, otc - when using, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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

Question Or Comments?

1-800-56-ORALB
http://www.oralb.com

Other

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

© Oral-B Laboratories

Made in Colombia

Principal Display Panel - 500Ml Label

Oral -B®

Anti-Bacterial Rinse

  • Dual action formula kills
    plaque and bad breath
    bacteria on contact
  • NATURAL
    MINT
    FLAVOR

    16.9 oz / 500ml

    Principal Display Panel (500ml Label)

    Principal Display Panel (500ml Label)

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