NDC Package 57896-565-12 Heartburn Relief

Aluminum Hydroxide And Magnesium Carbonate Suspension 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:
57896-565-12
Package Description:
355 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Heartburn Relief
Non-Proprietary Name:
Aluminum Hydroxide And Magnesium Carbonate
Substance Name:
Aluminum Hydroxide; Magnesium Carbonate
Usage Information:
Shake well before useadults and children 12 years and older take 2-4 teaspoonsful four times a day or as directed by a doctorchildren under 12 years: consult a doctortake after meals and at bedtimedispense product only by spoon or other measuring device
11-Digit NDC Billing Format:
57896056512
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
355 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 245001 - aluminum hydroxide 254 MG / magnesium carbonate 237.5 MG in 5 mL Oral Suspension
  • RxCUI: 245001 - aluminum hydroxide 50.8 MG/ML / magnesium carbonate 47.5 MG/ML Oral Suspension
  • RxCUI: 245001 - aluminum hydroxide 254 MG / magnesium carbonate 237.5 MG per 5 ML Oral Suspension
Product Type:
Human Otc Drug
Labeler Name:
Geri-care Pharmaceuticals, Corp
Dosage Form:
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
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:
07-01-2024
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.

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Frequently Asked Questions

What is NDC 57896-565-12?

The NDC Packaged Code 57896-565-12 is assigned to a package of 355 ml in 1 bottle of Heartburn Relief, a human over the counter drug labeled by Geri-care Pharmaceuticals, Corp. The product's dosage form is suspension and is administered via oral form.This product is billed per "ML" milliliter and contains an estimated amount of 355 billable units per package.

Is NDC 57896-565 included in the NDC Directory?

Yes, Heartburn Relief with product code 57896-565 is active and included in the NDC Directory. The product was first marketed by Geri-care Pharmaceuticals, Corp on July 01, 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 NDC billing unit for package 57896-565-12?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 355.

What is the 11-digit format for NDC 57896-565-12?

The 11-digit format is 57896056512. 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
5-3-257896-565-125-4-257896-0565-12