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  5. NDC Package Code: 17856-6833-1 Mi Acid

NDC Package 17856-6833-1 Mi Acid

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
17856-6833-1
Package Description:
50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 30 mL in 1 CUP, UNIT-DOSE
Product Code:
17856-6833
Proprietary Name:
Mi Acid
Usage Information:
•shake well before use•measure with dosing cup provided•adults and children 12 years and over: 10 mL – 20 mL between meals, at bedtime or as directed by a doctor•do not take more than 120 mL in any 24 hour period•do not use the maximum dosage for more than 2 weeks•children under 12 years: ask a doctor•mL = milliliter
11-Digit NDC Billing Format:
17856683301
NDC to RxNorm Crosswalk:
  • RxCUI: 210036 - Mi-Acid 200 MG / 200 MG / 20 MG in 5 mL Oral Suspension
  • RxCUI: 210036 - aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML / simethicone 4 MG/ML Oral Suspension [Mi-Acid]
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 200 MG / magnesium hydroxide 200 MG / simethicone 20 MG) per 5 ML Oral Suspension
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 40 MG / magnesium hydroxide 40 MG / simethicone 4 MG) per ML Oral Suspension
  • RxCUI: 210036 - Mi-Acid (aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG) per 10 ML Oral Suspension
Labeler Name:
Atlantic Biologicals Corp.
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:
12-28-2018
Listing Expiration Date:
12-31-2021
Exclude Flag:
I
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 17856-6833-1?

The NDC Packaged Code 17856-6833-1 is assigned to a package of 50 cup, unit-dose in 1 box, unit-dose / 30 ml in 1 cup, unit-dose of Mi Acid, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

Is NDC 17856-6833 included in the NDC Directory?

No, Mi Acid with product code 17856-6833 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on December 28, 2018 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 17856-6833-1?

The 11-digit format is 17856683301. 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
5-4-117856-6833-15-4-217856-6833-01