Triple Antibiotic First Aid Antibiotic Ointment
NDC Package 52000-056-02
Package Information
Triple Antibiotic First Aid Antibiotic (bacitracin zinc, neomycin and polymyxin b sulfate) ointment is usesfirst aid to help prevent infection inminor cutsscrapesburns. This formulation utilizes a ointment delivery system. Marketed by Universal Distribution Center Llc, this product is identified by NDC 52000-056 and is authorized under FDA application M004.
Identification & Billing
- RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment
- RxCUI: 204602 - bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment
- RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 52000 - Universal Distribution Center Llc
- 52000-056 - Triple Antibiotic First Aid Antibiotic
- 52000-056-02 - 1 TUBE in 1 BOX / 14 g in 1 TUBE
- 52000-056 - Triple Antibiotic First Aid Antibiotic
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.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 52000-056-02 identifies a specific commercial package of 1 tube in 1 box / 14 g in 1 tube of Triple Antibiotic First Aid Antibiotic, a human over the counter drug labeled by Universal Distribution Center Llc. This ointment is formulated for topical use and contains bacitracin zinc; neomycin sulfate; polymyxin b sulfate 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 Universal Distribution Center Llc on December 09, 2020. The current certification is valid through December 31, 2026.
How is this Universal Distribution Center Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 52000005602. 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.