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  5. NDC Package Code: 11822-0213-4 Anticavity

NDC Package 11822-0213-4 Anticavity

Sodium Fluoride Rinse Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
11822-0213-4
Package Description:
532 mL in 1 BOTTLE, PLASTIC
Product Code:
11822-0213
Proprietary Name:
Anticavity
Non-Proprietary Name:
Sodium Fluoride
Substance Name:
Sodium Fluoride
Usage Information:
•adults and children 6 years of age and older: use once a day for brushing your teeth with a toothpaste•remove cap•pour 10 milliliters (10 mL mark on inside of cap) do not fill above 10 mL mark• vigorously swish 10 milliliter of rinse between your teeth for 1 minute and then spit out•do not swallow the rinse•do not eat or drink for 30 minutes after rinsing•instruct children under 12 years of 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:
11822021304
NDC to RxNorm Crosswalk:
  • RxCUI: 240698 - sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse
  • RxCUI: 240698 - sodium fluoride 0.5 MG/ML Mouthwash
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Rite Aid
    Dosage Form:
    Rinse - A liquid used to cleanse by flushing.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SODIUM FLUORIDE .2 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    part355
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    02-25-2005
    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 11822-0213-4?

    The NDC Packaged Code 11822-0213-4 is assigned to a package of 532 ml in 1 bottle, plastic of Anticavity, a human over the counter drug labeled by Rite Aid. The product's dosage form is rinse and is administered via oral form.

    Is NDC 11822-0213 included in the NDC Directory?

    Yes, Anticavity with product code 11822-0213 is active and included in the NDC Directory. The product was first marketed by Rite Aid on February 25, 2005 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 11822-0213-4?

    The 11-digit format is 11822021304. 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 5-4-1 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
    5-4-111822-0213-45-4-211822-0213-04