Mintox Maximum Strength Suspension
NDC Package 17856-5725-3

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Mintox Maximum Strength (aluminum hydroxide, magnesium hydroxide, dimethicone) suspension is • shake well before use• do not take more than 8 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks• adults and children 12 years and older: take 2 to 4 teaspoonfuls two times a day, or as directed by a doctor• children under 12 years: ask a doctor. This formulation utilizes a suspension delivery system. Marketed by Atlantic Biologicals Corp., this product is identified by NDC 17856-5725 and is authorized under FDA application M.

Identification & Billing

NDC Package Code
17856-5725-3
Package Description
30 mL in 1 CUP
Product Code
17856-5725
11-Digit Billing Format
17856572503
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
30 ML
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

Clinical Specifications

Proprietary Name
Mintox Maximum Strength
Non-Proprietary Name
Aluminum Hydroxide, Magnesium Hydroxide, Dimethicone
Substance Name
Aluminum Hydroxide; Dimethicone; Magnesium Hydroxide
Dosage Form
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
• shake well before use• do not take more than 8 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks• adults and children 12 years and older: take 2 to 4 teaspoonfuls two times a day, or as directed by a doctor• children under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Atlantic Biologicals Corp.
Product Type
Human Otc Drug
FDA Application #
M
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-01-2011
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (17856-5725). Click a package code to view its specific billing and regulatory data.

17856-5725-1
15 mL in 1 CUP

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 17856-5725-3 identifies a specific commercial package of 30 ml in 1 cup of Mintox Maximum Strength, a human over the counter drug labeled by Atlantic Biologicals Corp.. This product is billed per "ML" milliliter and contains an estimated amount of 30 billable units per package. This suspension is formulated for oral use and contains aluminum hydroxide; dimethicone; magnesium hydroxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Atlantic Biologicals Corp. on February 01, 2011. The current certification is valid through December 31, 2026.

How is this Atlantic Biologicals Corp. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17856572503. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 30 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
17856-5725-3
11-Digit CMS (5-4-2)
17856-5725-03

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.