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United States· US:79481-0835_e8b73739-d1b5-41ac-b931-1374915200f9

meijer EXTRA STRENGTH Gas Relief

A medicinal product containing dimethicone, unspecified, registered in United States by Meijer, 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…normalisedmeijer EXTRA STRENGTH Gas ReliefATC—REGISTER NO.US:79481-0835_e8b7373…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DIMETHICONE, UNSPECIFIED
Manufacturer
Meijer, 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 · 4

  • ndc11
    7948108355
    2 BLISTER PACK in 1 CARTON (79481-0835-5) / 25 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • ndc11
    7948108357
    3 BLISTER PACK in 1 CARTON (79481-0835-7) / 25 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • ndc11
    79481-0835-5
  • ndc11
    79481-0835-7

Regulatory notes

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

Same medicine, other countries

Dimethicone, unspecified in 6 other countries

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

All dimethicone, unspecified products

Authorised across Europe · EMA

The same active substance is authorised in 6 EEA countries. Names it is sold under:

  • Germany · Sab Simplex
  • Finland · Cuplaton
  • France · Polysilane
  • United Kingdom (Northern Ireland) · Hedrin
  • Ireland · Dentinox Infant Colic Drops
  • Poland · Esputicon

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/fad8cd55-2e2c-4763-9292-8c964c1aa69a
GET /v1/drugs/fad8cd55-2e2c-4763-9292-8c964c1aa69a?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": "125",
  "substance": "DIMETHICONE, UNSPECIFIED",
  "productndc": "79481-0835",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "M002",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about dimethicone, unspecified.

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.