Burn First Aid Cream
NDC Package 67777-007-52
Package Information
Burn First Aid cream is adults and children 2 years and over:clean the affected areaapply a small amount of this product on the area 3 to 4 times dailymay be covered with a sterile bandageChildren under 2 years:consult a doctor. This formulation utilizes a cream delivery system. Marketed by Dynarex Corporation, this product is identified by NDC 67777-007 and is authorized under FDA application M017.
Identification & Billing
- RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
- RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
- RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 67777 - Dynarex Corporation
- 67777-007 - Burn First Aid
- 67777-007-52 - 1000 BOX in 1 CASE / 10 PACKET in 1 BOX (67777-007-51) / 900 mg in 1 PACKET
- 67777-007 - Burn First Aid
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 (67777-007). 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 67777-007-52 identifies a specific commercial package of 1000 box in 1 case / 10 packet in 1 box (67777-007-51) / 900 mg in 1 packet of Burn First Aid, a human over the counter drug labeled by Dynarex Corporation. This cream is formulated for topical use and contains benzalkonium chloride; lidocaine hydrochloride 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 Dynarex Corporation on September 17, 2018. The current certification is valid through December 31, 2026.
How is this Dynarex Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 67777000752. 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.