Back to search

United States· US:62372-500_28fefbe1-4ae0-8558-e063-6394a90ad25a

Mylanta Maximum Strength Classic Flavor

A medicinal product containing aluminum hydroxide; magnesium hydroxide; dimethicone, registered in United States by Infirst Healthcare Inc..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedMylanta Maximum Strength Classic Flav…ATC—REGISTER NO.US:62372-500_28fefbe1…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
Manufacturer
Infirst Healthcare Inc.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 6

  • ndc11
    62372-500-10
  • ndc11
    62372-500-12
  • ndc11
    62372-500-30
  • ndc11
    6237250030
    295 mL in 1 BOTTLE, PLASTIC (62372-500-30)
  • ndc11
    6237250010
    100 mL in 1 BOTTLE, PLASTIC (62372-500-10)
  • ndc11
    6237250012
    355 mL in 1 BOTTLE, PLASTIC (62372-500-12)

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Aluminum hydroxide; magnesium hydroxide; dimethicone in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All aluminum hydroxide; magnesium hydroxide; dimethicone products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Cyprus · Maalox Plus
  • Greece · Maalox Plus, Zaxan
  • Italy · Maalox Plus

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/fa655a10-7d17-4202-88bf-5ee116e13190
GET /v1/drugs/fa655a10-7d17-4202-88bf-5ee116e13190?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "800; 800; 80",
  "substance": "ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE",
  "productndc": "62372-500",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "strength_unit": "mg/10mL; mg/10mL; mg/10mL",
  "application_number": "M001",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about aluminum hydroxide; magnesium hydroxide; dimethicone.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.