Hydrocortisone Acetate Pramoxine Hcl Cream
NDC Package 52817-817-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Hydrocortisone Acetate Pramoxine Hcl cream is topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. This formulation utilizes a cream delivery system. Marketed by Trupharma, Llc, this product is identified by NDC 52817-817.

Identification & Billing

NDC Package Code
52817-817-01
Package Description
1 TUBE in 1 CARTON / 28.4 g in 1 TUBE
Product Code
52817-817
11-Digit Billing Format
52817081701
RxNorm Crosswalk
  • RxCUI: 1234506 - hydrocortisone acetate 2.5 % / pramoxine HCl 1 % Topical Cream
  • RxCUI: 1234506 - hydrocortisone acetate 25 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream
  • RxCUI: 1234506 - hydrocortisone acetate 2.5 % / pramoxine hydrochloride 1 % Topical Cream

Clinical Specifications

Proprietary Name
Hydrocortisone Acetate Pramoxine Hcl
Non-Proprietary Name
Hydrocortisone Acetate, Pramoxine Hcl
Substance Name
Hydrocortisone Acetate; Pramoxine Hydrochloride
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Regulatory & Marketing

Labeler Name
Trupharma, Llc
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
11-19-2020
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 52817-817-01 identifies a specific commercial package of 1 tube in 1 carton / 28.4 g in 1 tube of Hydrocortisone Acetate Pramoxine Hcl, a human prescription drug labeled by Trupharma, Llc. This cream is formulated for topical use and contains hydrocortisone acetate; pramoxine 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 Trupharma, Llc on November 19, 2020. The current certification is valid through December 31, 2026.

How is this Trupharma, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52817081701. 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:

10-Digit Format (5-3-2)
52817-817-01
11-Digit CMS (5-4-2)
52817-0817-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.