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  5. NDC Package Code: 50967-357-60 Procort

NDC Package 50967-357-60 Procort

1.85% Hydrocortisone Acetate - 1.15% Pramoxine Hci Cream Cream Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50967-357-60
Package Description:
1 TUBE, WITH APPLICATOR in 1 CARTON / 1 TUBE, WITH APPLICATOR in 1 TUBE, WITH APPLICATOR / 60 g in 1 TUBE, WITH APPLICATOR
Product Code:
50967-357
Proprietary Name:
Procort
Non-Proprietary Name:
1.85% Hydrocortisone Acetate - 1.15% Pramoxine Hci Cream
Substance Name:
Hydrocortisone Acetate; Pramoxine Hydrochloride
Usage Information:
This combination medication is used to treat minor pain, itching, swelling, and discomfort caused by hemorrhoids and other problems of the anal area (e.g., anal fissures, itching). This medication contains pramoxine, an anesthetic that works by temporarily numbing the area. This product also contains hydrocortisone, a corticosteroid that reduces redness, itching, and swelling.
11-Digit NDC Billing Format:
50967035760
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
60 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 1114854 - hydrocortisone acetate 1.85 % / pramoxine HCl 1.15 % Rectal Cream
  • RxCUI: 1114854 - hydrocortisone acetate 18.5 MG/ML / pramoxine hydrochloride 11.5 MG/ML Rectal Cream
  • RxCUI: 1115730 - ProCort 1.85 % / 1.15 % Rectal Cream
  • RxCUI: 1115730 - hydrocortisone acetate 18.5 MG/ML / pramoxine hydrochloride 11.5 MG/ML Rectal Cream [Procort 1.85/1.15]
  • RxCUI: 1115730 - Procort 1.85 % / 1.15 % (hydrocortisone acetate / pramoxine HCl) Rectal Cream
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Womens Choice Pharmaceuticals Llc
    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(s):
  • 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):
  • HYDROCORTISONE ACETATE 18.5 mg/g
  • PRAMOXINE HYDROCHLORIDE 11.5 mg/g
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    06-30-2011
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 50967-357-60?

    The NDC Packaged Code 50967-357-60 is assigned to a package of 1 tube, with applicator in 1 carton / 1 tube, with applicator in 1 tube, with applicator / 60 g in 1 tube, with applicator of Procort, a human prescription drug labeled by Womens Choice Pharmaceuticals Llc. The product's dosage form is cream and is administered via topical form.This product is billed per "GM" gram and contains an estimated amount of 60 billable units per package.

    Is NDC 50967-357 included in the NDC Directory?

    Yes, Procort with product code 50967-357 is active and included in the NDC Directory. The product was first marketed by Womens Choice Pharmaceuticals Llc on June 30, 2011 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 50967-357-60?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 60.

    What is the 11-digit format for NDC 50967-357-60?

    The 11-digit format is 50967035760. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-250967-357-605-4-250967-0357-60