Hemorrhoid Anesthetic Ointment
NDC Package 52000-057-01
Package Information
Hemorrhoid Anesthetic (mineral oil, petrolatum, phenylephrine hcl) ointment is usesFor the temporary relief of local anorectal burning and discomfort associated with hemmorrhoids, anorectal disorders, inflamed hemorrhoidal tissues or piles. This formulation utilizes a ointment delivery system. Marketed by Universal Distribution Center Llc, this product is identified by NDC 52000-057 and is authorized under FDA application M015.
Identification & Billing
- RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine HCl 0.25 % Rectal Ointment
- RxCUI: 1372298 - mineral oil 0.14 MG/MG / petrolatum 0.749 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Ointment
- RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine hydrochloride 0.25 % Rectal Ointment
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 52000 - Universal Distribution Center Llc
- 52000-057 - Hemorrhoid Anesthetic
- 52000-057-01 - 1 TUBE in 1 CARTON / 28 g in 1 TUBE
- 52000-057 - Hemorrhoid Anesthetic
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 (52000-057). 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 52000-057-01 identifies a specific commercial package of 1 tube in 1 carton / 28 g in 1 tube of Hemorrhoid Anesthetic, a human over the counter drug labeled by Universal Distribution Center Llc. This ointment is formulated for topical use and contains mineral oil; petrolatum; phenylephrine 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 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: 52000005701. 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.