Hydrogen Peroxide Solution
NDC Package 37808-871-72
Package Information
Hydrogen Peroxide solution is first Aid Antiseptic:clean the affected areaapply a small amount of the product on the affected area 1 to 3 times a daymay be covered with a sterile bandageif bandaged, let dry firstOral Debriding Agent: adults, children over 2 years of age:mix with equal amount of waterswish around in the mouth over the affected area for at least 1 minute, then spit outuse up to 4 times daily after meals and at bedtimechildren under 12 years of age should be supervised in the usechildren under 2 years of age: consult a dentist or doctor. This formulation utilizes a solution delivery system. Marketed by H E B, this product is identified by NDC 37808-871 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
- 37808 - H E B
- 37808-871 - Hydrogen Peroxide
- 37808-871-72 - 296 mL in 1 BOTTLE, SPRAY
- 37808-871 - 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.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (37808-871). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 37808-871-72 identifies a specific commercial package of 296 ml in 1 bottle, spray of Hydrogen Peroxide, a human over the counter drug labeled by H E B. 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 H E B on July 15, 2015. The current certification is valid through December 31, 2027.
How is this H E B product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808087172. 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.