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United States· US:37808-510_bc8f027b-369d-4296-bd48-e6e12d5e79a1

HEB Extra Strength

A medicinal product containing aluminum hydroxide; magnesium carbonate, registered in United States by HEB.

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedHEB Extra StrengthATC—REGISTER NO.US:37808-510_bc8f027b…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
Manufacturer
HEB
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 · 1

  • ndc11
    37808-510-10

Regulatory notes

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

Same medicine, other countries

Aluminum hydroxide; magnesium carbonate in 9 other countries

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

All aluminum hydroxide; magnesium carbonate products

Authorised across Europe · EMA

The same active substance is authorised in 17 EEA countries. Names it is sold under:

  • Bulgaria · Алмагел
  • Cyprus · Maalox
  • Czechia · Maalox
  • Germany · Maaloxan
  • Estonia · Maalox, Maalox (Suhkruvabad)
  • France · Maalox Maux D’estomac, Maalox Maux D’estomac Fruits Rouges
  • United Kingdom (Northern Ireland) · Maalox
  • Greece · Aludrox, Maalox
  • Ireland · Maalox
  • Italy · Maalox, Maalox Aroma Menta
  • Lithuania · Maalox, Maalox (Be Cukraus)
  • Latvia · Maalox, Maalox (Nesatur Cukuru)
  • Netherlands · Aluminium Oxide/Magnesium Hydroxide Aurobindo, Antagel
  • Norway · Novaluzid
  • Poland · Maalox
  • Romania · Dicarbocalm Aromă De Lămâie, Dicarbocalm Cu Aromă De Coacăze Negre
  • Slovakia · Maalox, Maalox Bez Cukru S Príchuťou Citróna

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/c8470c13-13b4-4b7f-9fb5-1e9899e45150
GET /v1/drugs/c8470c13-13b4-4b7f-9fb5-1e9899e45150?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": "160; 105",
  "substance": "ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE",
  "productndc": "37808-510",
  "dosage_form": "TABLET, CHEWABLE",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1",
  "application_number": "M001",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about aluminum hydroxide; magnesium carbonate.

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.