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  5. NDC Package Code: 50066-065-30 Nasalub Nasal Relief

NDC Package 50066-065-30 Nasalub Nasal Relief

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
50066-065-30
Package Description:
1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Code:
50066-065
Proprietary Name:
Nasalub Nasal Relief
Usage Information:
Directionsadults and children 6 to 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour periodchildren under 6 years of age: ask a doctorshake well before use. To open, rotate cap to align the marks. squeeze cap on both sides in a counterclockwise turn and pull off to remove. To spray, remove clamp and hold bottle with thumb at base and nozzle between first and second fingers. Without tiliting the head, insert nozzle into nostril. Fully depress rim with a firm, een stroke and sniff deeply. Wipe nozzle clean after each use and sanp cab back onto the bottle.
11-Digit NDC Billing Format:
50066006530
NDC to RxNorm Crosswalk:
  • RxCUI: 1000990 - oxymetazoline HCl 0.05 % Nasal Spray
  • RxCUI: 1000990 - oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray
  • RxCUI: 1000990 - oxymetazoline hydrochloride 0.05 % Nasal Spray
    • Labeler Name:
    Genomma Lab Usa, Inc
    Sample Package:
    No
    Start Marketing Date:
    12-02-2014
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    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 50066-065-30?

    The NDC Packaged Code 50066-065-30 is assigned to a package of 1 bottle in 1 carton / 30 ml in 1 bottle of Nasalub Nasal Relief, labeled by Genomma Lab Usa, Inc. The product's dosage form is and is administered via form.

    Is NDC 50066-065 included in the NDC Directory?

    No, Nasalub Nasal Relief with product code 50066-065 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Genomma Lab Usa, Inc on December 02, 2014 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50066-065-30?

    The 11-digit format is 50066006530. 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
    5-3-250066-065-305-4-250066-0065-30