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  5. NDC Package Code: 0135-0098-26 Gaviscon Extra Strength

NDC Package 0135-0098-26 Gaviscon Extra Strength

Aluminum Hydroxide And Magnesium Carbonate Tablet, Chewable 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:
0135-0098-26
Package Description:
100 TABLET, CHEWABLE in 1 BOTTLE
Product Code:
0135-0098
Proprietary Name:
Gaviscon Extra Strength
Non-Proprietary Name:
Aluminum Hydroxide And Magnesium Carbonate
Substance Name:
Aluminum Hydroxide; Magnesium Carbonate
Usage Information:
This medication is used to treat the symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Aluminum and magnesium antacids work quickly to lower the acid in the stomach. Liquid antacids usually work faster/better than tablets or capsules. This medication works only on existing acid in the stomach. It does not prevent acid production. It may be used alone or with other medications that lower acid production (including H2 blockers such as cimetidine/ranitidine and proton pump inhibitors such as omeprazole).
11-Digit NDC Billing Format:
00135009826
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1086458 - Gavsicon Regular Strength 80 MG / 14.2 MG Chewable Tablet
  • RxCUI: 1086458 - aluminum hydroxide 80 MG / magnesium trisilicate 14.2 MG Chewable Tablet [Gaviscon Chewable]
  • RxCUI: 1086458 - Gaviscon Chewable 80/14.2 (aluminum hydroxide / magnesium trisilicate) Chewable Tablet
  • RxCUI: 1086458 - Gaviscon Chewable 80/14.2 Chewable Tablet
  • RxCUI: 1086458 - Gavsicon Regular Strength (aluminum hydroxide 80 MG / magnesium trisilicate 14.2 MG) Chewable Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Glaxosmithkline Consumer Healthcare Holdings (us) Llc
    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.
    • Active Ingredient(s):
  • ALUMINUM HYDROXIDE 160 mg/1
  • MAGNESIUM CARBONATE 105 mg/1
    • Sample Package:
    No
    FDA Application Number:
    part331
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-13-2011
    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 0135-0098-26?

    The NDC Packaged Code 0135-0098-26 is assigned to a package of 100 tablet, chewable in 1 bottle of Gaviscon Extra Strength, a human over the counter drug labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 0135-0098 included in the NDC Directory?

    Yes, Gaviscon Extra Strength with product code 0135-0098 is active and included in the NDC Directory. The product was first marketed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc on June 13, 2011 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 NDC billing unit for package 0135-0098-26?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

    What is the 11-digit format for NDC 0135-0098-26?

    The 11-digit format is 00135009826. 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 4-4-2 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
    4-4-20135-0098-265-4-200135-0098-26