NDC Package 76168-601-01 Nasal Decongestant Original

View Billable Units, 11-Digit Format, RxNorm

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:
76168-601-01
Package Description:
1 BOTTLE, PUMP in 1 CARTON / 30 mL in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Nasal Decongestant Original
Usage Information:
Adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.Children under 6 years of age: ask a doctor.Shake well before use. Before using the first time, remove the protective cap from the tip and prime metered pump by depressing pump firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozzle clean after use.
11-Digit NDC Billing Format:
76168060101
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:
    Velocity Pharma Llc
    Sample Package:
    No
    Start Marketing Date:
    05-29-2019
    Listing Expiration Date:
    12-31-2020
    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 76168-601-01?

    The NDC Packaged Code 76168-601-01 is assigned to a package of 1 bottle, pump in 1 carton / 30 ml in 1 bottle, pump of Nasal Decongestant Original, labeled by Velocity Pharma Llc. The product's dosage form is and is administered via form.

    Is NDC 76168-601 included in the NDC Directory?

    No, Nasal Decongestant Original with product code 76168-601 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Velocity Pharma Llc on May 29, 2019 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 76168-601-01?

    The 11-digit format is 76168060101. 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
    5-3-276168-601-015-4-276168-0601-01