NDC Package 77982-001-01 Optirinse Plus

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:
77982-001-01
Package Description:
500 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Optirinse Plus
Usage Information:
 Adults and children 6 years of age and olderUse once a day after brushing your teeth with a toothpasteRemove capPour 10 milliliters into a cap (10 mL mark on inside of cap); do not fill above 10 mL markVigorously swish 10 milliliters of rinse between your teeth for 1 minute and then spit outDo not swallow the rinseDo not eat or drink for 30 minutes after rinsingInstruct children 12 years under age in good rinsing habits (to minimize swallowing)Supervise children as necessary until capable of using without supervision  Children under 6 years of age Consult a dentist or doctor
11-Digit NDC Billing Format:
77982000101
NDC to RxNorm Crosswalk:
  • RxCUI: 2467743 - cetylpyridinium chloride 0.05 % / sodium fluoride 0.05 % (fluoride ion 0.02 % ) Mouthwash
  • RxCUI: 2467743 - cetylpyridinium chloride 0.5 MG/ML / sodium fluoride 0.5 MG/ML Mouthwash
  • RxCUI: 2467743 - cetylpyridinium chloride 0.05 % / sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
  • Labeler Name:
    Laboratoires Msp Inc
    Sample Package:
    No
    Start Marketing Date:
    11-04-2020
    Listing Expiration Date:
    12-31-2021
    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 77982-001-01?

    The NDC Packaged Code 77982-001-01 is assigned to a package of 500 ml in 1 bottle of Optirinse Plus, labeled by Laboratoires Msp Inc. The product's dosage form is and is administered via form.

    Is NDC 77982-001 included in the NDC Directory?

    No, Optirinse Plus with product code 77982-001 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Laboratoires Msp Inc on November 04, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 77982-001-01?

    The 11-digit format is 77982000101. 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
    5-3-277982-001-015-4-277982-0001-01