NDC Package 24208-450-15 Advanced Eye Relief/ Redness Maximum Relief

Naphazoline Hydrochloride And Hypromellose Solution/ Drops Ophthalmic - 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:
24208-450-15
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 15 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Advanced Eye Relief/ Redness Maximum Relief
Non-Proprietary Name:
Naphazoline Hydrochloride And Hypromellose
Substance Name:
Hypromellose, Unspecified; Naphazoline Hydrochloride
Usage Information:
•instill 1 to 2 drops in the affected eye(s) up to four times daily
11-Digit NDC Billing Format:
24208045015
NDC to RxNorm Crosswalk:
  • RxCUI: 1046654 - hypromellose 0.5 % / naphazoline HCl 0.03 % Ophthalmic Solution
  • RxCUI: 1046654 - hypromellose 5 MG/ML / naphazoline hydrochloride 0.3 MG/ML Ophthalmic Solution
  • RxCUI: 1046654 - hypromellose 0.5 % / naphazoline hydrochloride 0.03 % Ophthalmic Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Bausch & Lomb Incorporated
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Sample Package:
    No
    FDA Application Number:
    part349
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    09-02-2010
    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 24208-450-15?

    The NDC Packaged Code 24208-450-15 is assigned to a package of 1 bottle, dropper in 1 carton / 15 ml in 1 bottle, dropper of Advanced Eye Relief/ Redness Maximum Relief, a human over the counter drug labeled by Bausch & Lomb Incorporated. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 24208-450 included in the NDC Directory?

    Yes, Advanced Eye Relief/ Redness Maximum Relief with product code 24208-450 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incorporated on September 02, 2010 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 24208-450-15?

    The 11-digit format is 24208045015. 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
    5-3-224208-450-155-4-224208-0450-15