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  5. NDC Package Code: 41163-004-77 Anticavity

NDC Package 41163-004-77 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:
41163-004-77
Package Description:
500 mL in 1 BOTTLE, PLASTIC
Product Code:
41163-004
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 after brushing your teeth with toothpasteremove cappour 10 milliliters (10 mL mark on inside of cap); do not fill above 10 mL markvigorously swish 10 millilitrs of rinse between your teeth for 1 minute then spit outdo not swallow the rinsedo not eat or drink for 30 miutes after rinsinginstruct children under 12 years of age in good rinsing habits (to minimize swallowing)supervise children as necessary until capable of using without supervisionchildren under 6 year of age: consult a dentist or doctor
11-Digit NDC Billing Format:
41163000477
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:
    United Natural Foods, Inc. Dba Unfi
    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:
    M021
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-17-2011
    Listing Expiration Date:
    12-31-2025
    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 41163-004-77?

    The NDC Packaged Code 41163-004-77 is assigned to a package of 500 ml in 1 bottle, plastic of Anticavity, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. The product's dosage form is rinse and is administered via oral form.

    Is NDC 41163-004 included in the NDC Directory?

    Yes, Anticavity with product code 41163-004 is active and included in the NDC Directory. The product was first marketed by United Natural Foods, Inc. Dba Unfi on August 17, 2011 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41163-004-77?

    The 11-digit format is 41163000477. 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
    5-3-241163-004-775-4-241163-0004-77