NDC Package 69423-829-06 Rolaids Ultra Strength Antacid Strawberry

Calcium Carbonate,Magnesium Hydroxide Tablet, Chewable Oral - View Billable Units, 11-Digit Format, RxNorm

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:
69423-829-06
Package Description:
1 PACKAGE in 1 CARTON / 6 TABLET, CHEWABLE in 1 PACKAGE
Product Code:
Proprietary Name:
Rolaids Ultra Strength Antacid Strawberry
Non-Proprietary Name:
Calcium Carbonate, Magnesium Hydroxide
Substance Name:
Calcium Carbonate; Magnesium Hydroxide
Usage Information:
Chew 2-3 chews as symptoms occur, or as directed by a doctor  
11-Digit NDC Billing Format:
69423082906
NDC to RxNorm Crosswalk:
  • RxCUI: 1607295 - calcium carbonate 1330 MG / magnesium hydroxide 235 MG Chewable Tablet
  • RxCUI: 1607295 - calcium carbonate 1330 MG (Ca 535 MG) / magnesium hydroxide 235 MG (Mg 100 MG) Chewable Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    The Procter & Gamble Manufacturing Company
    Dosage Form:
    Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M001
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-30-2024
    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 69423-829-06?

    The NDC Packaged Code 69423-829-06 is assigned to a package of 1 package in 1 carton / 6 tablet, chewable in 1 package of Rolaids Ultra Strength Antacid Strawberry, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 69423-829 included in the NDC Directory?

    Yes, Rolaids Ultra Strength Antacid Strawberry with product code 69423-829 is active and included in the NDC Directory. The product was first marketed by The Procter & Gamble Manufacturing Company on January 30, 2024 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 69423-829-06?

    The 11-digit format is 69423082906. 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
    5-3-269423-829-065-4-269423-0829-06