NDC Package 55910-638-12 Maximum Strength Advanced Antacid

Aluminum Hydroxide,Magnesium Hydroxide,Simethicone Liquid 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:
55910-638-12
Package Description:
355 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Maximum Strength Advanced Antacid
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 of age and older: take 10ml to 20ml (1 to 2 doses) two times a day or as directed by a doctordo not exceed 40ml (4 doses) in a 24 hour period or use the maximum dosage for more than 2 weekschildren under 12 years of age: ask a doctor
11-Digit NDC Billing Format:
55910063812
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:
    Dolgencorp, Llc
    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.
  • Sample Package:
    No
    FDA Application Number:
    M001
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-01-2021
    Listing Expiration Date:
    12-31-2024
    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 55910-638-12?

    The NDC Packaged Code 55910-638-12 is assigned to a package of 355 ml in 1 bottle of Maximum Strength Advanced Antacid, a human over the counter drug labeled by Dolgencorp, Llc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 55910-638 included in the NDC Directory?

    Yes, Maximum Strength Advanced Antacid with product code 55910-638 is active and included in the NDC Directory. The product was first marketed by Dolgencorp, Llc on February 01, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55910-638-12?

    The 11-digit format is 55910063812. 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
    5-3-255910-638-125-4-255910-0638-12