1. Home
  2. Labeler Index
  3. Meda Pharmaceuticals Inc.
  4. 0037-6824
  5. NDC Package Code: 0037-6824-10 Epifoam

NDC Package 0037-6824-10 Epifoam

Pramoxine Hydrochloride And Hydrocortisone Acetate Aerosol, Foam 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:
0037-6824-10
Package Description:
1 CANISTER in 1 CARTON / 10 g in 1 CANISTER
Product Code:
0037-6824
Proprietary Name:
Epifoam
Non-Proprietary Name:
Pramoxine Hydrochloride And Hydrocortisone Acetate
Substance Name:
Hydrocortisone Acetate; Pramoxine Hydrochloride
Usage Information:
This product contains 2 medications. Pramoxine is an anesthetic that is used on the skin to relieve minor pain, itching, and discomfort. It works by temporarily numbing the area. Hydrocortisone is a corticosteroid that reduces redness, swelling, and itching. This combination medication is used to treat certain skin conditions such as eczema, psoriasis, rash, cuts, scrapes, insect bites, or minor burns. This product is available in different strengths and forms (e.g., aerosol foam, cream, ointment, lotion). The type of medication used depends on the location of your condition and the type of skin problem being treated. Creams are the most frequently used form. Lotions may be better for hairy areas. Ointments may be better for dry areas and when a stronger effect or skin protection is desired. Foams can be easier and less messy to apply.
11-Digit NDC Billing Format:
00037682410
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
10 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 904782 - hydrocortisone acetate 1 % / pramoxine HCl 1 % Topical Foam
  • RxCUI: 904782 - hydrocortisone acetate 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Foam
  • RxCUI: 904782 - hydrocortisone acetate 1 % / pramoxine hydrochloride 1 % Topical Foam
  • RxCUI: 904783 - epifoam 1 % / 1 % Topical Foam
  • RxCUI: 904783 - hydrocortisone acetate 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Foam [Epifoam]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Meda Pharmaceuticals Inc.
    Dosage Form:
    Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
    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 100 mg/10g
  • PRAMOXINE HYDROCHLORIDE 100 mg/10g
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA086457
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-25-2014
    Listing Expiration Date:
    12-31-2025
    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 0037-6824-10?

    The NDC Packaged Code 0037-6824-10 is assigned to a package of 1 canister in 1 carton / 10 g in 1 canister of Epifoam, a human prescription drug labeled by Meda Pharmaceuticals Inc.. The product's dosage form is aerosol, foam and is administered via topical form.

    Is NDC 0037-6824 included in the NDC Directory?

    Yes, Epifoam with product code 0037-6824 is active and included in the NDC Directory. The product was first marketed by Meda Pharmaceuticals Inc. on August 25, 2014 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0037-6824-10?

    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 10.

    What is the 11-digit format for NDC 0037-6824-10?

    The 11-digit format is 00037682410. 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 4-4-2 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
    4-4-20037-6824-105-4-200037-6824-10