warnings
Warnings Ask a doctor before use if you have kidney disease a magnesium restricted diet Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
Mylanta One Antacid/Anti-Gas
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Mylanta One Antacid/Anti-Gas
- Generic name
- CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, DIMETHICONE
- Manufacturer
- Infirst Healthcare Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ed1b03f0-fabc-4c1c-8e6d-9f15c380300c
- SPL ID
- 0c4462a1-c735-c0ec-e063-6294a90a5e0c
- Version
- 3
- Effective date
- 2023-12-11
- Source export date
- 2026-10-30
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:44:04
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M001 | openfda.application_number | |
| brand name | Mylanta One Antacid/Anti-Gas | openfda.brand_name | |
| generic name | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, DIMETHICONE | openfda.generic_name | |
| manufacturer name | Infirst Healthcare Inc. | openfda.manufacturer_name | |
| ndc | package | 62372-552-50 | openfda.package_ndc |
| ndc | package | 62372-552-51 | openfda.package_ndc |
| ndc | product | 62372-552 | openfda.product_ndc |
| ndc11 | package | 62372055251 | derived:openfda.package_ndc |
| ndc11 | package | 62372055250 | derived:openfda.package_ndc |
| rxcui | 2556794 | openfda.rxcui | |
| spl id | 0c4462a1-c735-c0ec-e063-6294a90a5e0c | id | |
| spl set id | ed1b03f0-fabc-4c1c-8e6d-9f15c380300c | set_id | |
| unii | NBZ3QY004S | openfda.unii | |
| unii | H0G9379FGK | openfda.unii | |
| unii | 92RU3N3Y1O | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.