Hydrogen Peroxide Solution
NDC Package 67751-001-04
Package Information
Hydrogen Peroxide solution is first aid antiseptic:clean the affected areaapply a small amount of product on the area 1 to 3 times dailymay be covered with a sterile bandageif bandaged, let dry firstOral debriding agent (oral rinse):adults and children 2 years of age and over:mix with an equal amount of waterswish around in the mouth over the affected area for at least 1 minute and then spit outuse up to 4 times daily after meals and at bedtime or as directed by a dentist or doctorchildren under 12 years of age should be supervised in the use of this productchildren under 2 years of age: consult a dentist or doctor. This formulation utilizes a solution delivery system. Marketed by Navajo Manufacturing Company Inc., this product is identified by NDC 67751-001 and is authorized under FDA application M003.
Identification & Billing
- RxCUI: 91349 - hydrogen peroxide 3 % Topical Solution
- RxCUI: 91349 - hydrogen peroxide 30 MG/ML Topical Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 67751 - Navajo Manufacturing Company Inc.
- 67751-001 - Hydrogen Peroxide
- 67751-001-04 - 118 mL in 1 BOTTLE, PLASTIC
- 67751-001 - Hydrogen Peroxide
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 67751-001-04 identifies a specific commercial package of 118 ml in 1 bottle, plastic of Hydrogen Peroxide, a human over the counter drug labeled by Navajo Manufacturing Company Inc.. This solution is formulated for topical use and contains hydrogen peroxide as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Navajo Manufacturing Company Inc. on April 24, 2013. The current certification is valid through December 31, 2027.
How is this Navajo Manufacturing Company Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 67751000104. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.