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  5. NDC Package Code: 83324-122-12 Qch Maximum Strength Antacid 516

NDC Package 83324-122-12 Qch Maximum Strength Antacid 516

Aluminum Hydroxide,Magnesium Hydroxide,Simethicone Liquid 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:
83324-122-12
Package Description:
355 mL in 1 BOTTLE
Product Code:
83324-122
Proprietary Name:
Qch Maximum Strength Antacid 516
Non-Proprietary Name:
Aluminum Hydroxide, Magnesium Hydroxide, Simethicone
Substance Name:
Aluminum Hydroxide; Dimethicone; Magnesium Hydroxide
Usage Information:
Shake well before useadults and children 12 years and older: take 10 mL - 20 mL two times a day, or as directed by a doctorchildren under 12 years: consult a doctormL = milliliter
11-Digit NDC Billing Format:
83324012212
NDC to RxNorm Crosswalk:
  • RxCUI: 237870 - aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG in 5 mL Oral Suspension
  • RxCUI: 237870 - aluminum hydroxide 80 MG/ML / magnesium hydroxide 80 MG/ML / simethicone 8 MG/ML Oral Suspension
  • RxCUI: 237870 - aluminum hydroxide 2400 MG / magnesium hydroxide 2400 MG / dimethicone 240 MG per 30 ML Oral Suspension
  • RxCUI: 237870 - aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG per 5 ML Oral Suspension
  • RxCUI: 237870 - aluminum hydroxide 800 MG / magnesium hydroxide 800 MG / dimethicone 80 MG per 10 ML Oral Suspension
Product Type:
Human Otc Drug
Labeler Name:
Chain Drug Marketing Association Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M001
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-28-2024
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 83324-122-12?

The NDC Packaged Code 83324-122-12 is assigned to a package of 355 ml in 1 bottle of Qch Maximum Strength Antacid 516, a human over the counter drug labeled by Chain Drug Marketing Association Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 83324-122 included in the NDC Directory?

Yes, Qch Maximum Strength Antacid 516 with product code 83324-122 is active and included in the NDC Directory. The product was first marketed by Chain Drug Marketing Association Inc. on August 28, 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 83324-122-12?

The 11-digit format is 83324012212. 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
5-3-283324-122-125-4-283324-0122-12