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  5. NDC Package Code: 52000-022-39 Hydrocortisone Anti-itch

NDC Package 52000-022-39 Hydrocortisone Anti-itch

Hydrocortisone Cream Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
52000-022-39
Package Description:
1 TUBE in 1 BOX / 14 g in 1 TUBE (52000-022-38)
Product Code:
52000-022
Proprietary Name:
Hydrocortisone Anti-itch
Non-Proprietary Name:
Hydrocortisone
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:
52000002239
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Universal Distribution Center 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.
  • 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(es):
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-09-2020
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
52000-022-371 TUBE in 1 BOX / 14 g in 1 TUBE (52000-022-36)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52000-022-39?

The NDC Packaged Code 52000-022-39 is assigned to a package of 1 tube in 1 box / 14 g in 1 tube (52000-022-38) of Hydrocortisone Anti-itch, a human over the counter drug labeled by Universal Distribution Center Llc. The product's dosage form is cream and is administered via topical form.

Is NDC 52000-022 included in the NDC Directory?

Yes, Hydrocortisone Anti-itch with product code 52000-022 is active and included in the NDC Directory. The product was first marketed by Universal Distribution Center Llc on December 09, 2020 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 52000-022-39?

The 11-digit format is 52000002239. 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
5-3-252000-022-395-4-252000-0022-39