NDC Package 41250-290-04 Hydrocortisone

Hydrocortisone Continuous Spray Aerosol, Spray Topical - View Billable Units, 11-Digit Format, RxNorm

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:
41250-290-04
Package Description:
113 g in 1 CAN
Product Code:
Proprietary Name:
Hydrocortisone
Non-Proprietary Name:
Hydrocortisone Continuous Spray
Substance Name:
Hydrocortisone
Usage Information:
This medication is used to treat a variety of skin conditions (e.g., insect bites, poison oak/ivy, eczema, dermatitis, allergies, rash, itching of the outer female genitals, anal itching). Hydrocortisone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a mild corticosteroid.
11-Digit NDC Billing Format:
41250029004
NDC to RxNorm Crosswalk:
  • RxCUI: 317564 - hydrocortisone 1 % Topical Spray
  • RxCUI: 317564 - hydrocortisone 10 MG/ML Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer Distribution Inc.
    Dosage Form:
    Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
    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):
    Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-01-2021
    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 41250-290-04?

    The NDC Packaged Code 41250-290-04 is assigned to a package of 113 g in 1 can of Hydrocortisone, a human over the counter drug labeled by Meijer Distribution Inc.. The product's dosage form is aerosol, spray and is administered via topical form.

    Is NDC 41250-290 included in the NDC Directory?

    Yes, Hydrocortisone with product code 41250-290 is active and included in the NDC Directory. The product was first marketed by Meijer Distribution Inc. on March 01, 2021 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 11-digit format for NDC 41250-290-04?

    The 11-digit format is 41250029004. 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
    5-3-241250-290-045-4-241250-0290-04