NDC Package 71403-003-15 Rhofade

Oxymetazoline Hydrochloride Cream 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:
71403-003-15
Package Description:
1 TUBE in 1 CARTON / 3 g in 1 TUBE
Product Code:
Proprietary Name:
Rhofade
Non-Proprietary Name:
Oxymetazoline Hydrochloride
Substance Name:
Oxymetazoline Hydrochloride
Usage Information:
This medication is used to treat a certain skin disorder known as rosacea. It works by narrowing the blood vessels in the face. Oxymetazoline belongs to a class of drugs known as a sympathomimetic (alpha receptor agonist). It may help to decrease facial redness caused by rosacea.
11-Digit NDC Billing Format:
71403000315
NDC to RxNorm Crosswalk:
  • RxCUI: 1869816 - oxymetazoline HCl 1 % Topical Cream
  • RxCUI: 1869816 - oxymetazoline hydrochloride 10 MG/ML Topical Cream
  • RxCUI: 1869821 - Rhofade 1 % Topical Cream
  • RxCUI: 1869821 - oxymetazoline hydrochloride 10 MG/ML Topical Cream [Rhofade]
  • RxCUI: 1869821 - Rhofade 10 MG/ML Topical Cream
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Epi Health, 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.
  • Sample Package:
    No
    FDA Application Number:
    NDA208552
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-18-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    71403-003-301 TUBE in 1 CARTON / 30 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71403-003-15?

    The NDC Packaged Code 71403-003-15 is assigned to a package of 1 tube in 1 carton / 3 g in 1 tube of Rhofade, a human prescription drug labeled by Epi Health, Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 71403-003 included in the NDC Directory?

    Yes, Rhofade with product code 71403-003 is active and included in the NDC Directory. The product was first marketed by Epi Health, Llc on January 18, 2021 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 11-digit format for NDC 71403-003-15?

    The 11-digit format is 71403000315. 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
    5-3-271403-003-155-4-271403-0003-15