NDC Package 17856-5725-1 Mintox Maximum Strength

Aluminum Hydroxide,Magnesium Hydroxide,Dimethicone 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:
17856-5725-1
Package Description:
15 mL in 1 CUP
Product Code:
Proprietary Name:
Mintox Maximum Strength
Non-Proprietary Name:
Aluminum Hydroxide, Magnesium Hydroxide, Dimethicone
Substance Name:
Aluminum Hydroxide; Dimethicone; Magnesium Hydroxide
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
11-Digit NDC Billing Format:
17856572501
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:
Atlantic Biologicals 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:
M
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-01-2011
Listing Expiration Date:
12-31-2026
Exclude Flag:
N

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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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
17856-5725-330 mL in 1 CUP

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Frequently Asked Questions

What is NDC 17856-5725-1?

The NDC Packaged Code 17856-5725-1 is assigned to a package of 15 ml in 1 cup of Mintox Maximum Strength, a human over the counter drug labeled by Atlantic Biologicals Corp.. The product's dosage form is suspension and is administered via oral form.

Is NDC 17856-5725 included in the NDC Directory?

Yes, Mintox Maximum Strength with product code 17856-5725 is active and included in the NDC Directory. The product was first marketed by Atlantic Biologicals Corp. on February 01, 2011 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17856-5725-1?

The 11-digit format is 17856572501. 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 5-4-1 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
5-4-117856-5725-15-4-217856-5725-01