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
- aa694e0d-7891-4870-8106-dd57f1e29fb4
- SPL ID
- 0c441a11-2c3b-c0ef-e063-6294a90abc86
- Version
- 3
- Effective date
- 2023-12-11
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:56:45
| 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 | 62372-551-51 | openfda.package_ndc |
| ndc | package | 62372-551-50 | openfda.package_ndc |
| ndc | product | 62372-551 | openfda.product_ndc |
| ndc11 | package | 62372055150 | derived:openfda.package_ndc |
| ndc11 | package | 62372055151 | derived:openfda.package_ndc |
| rxcui | 2556794 | openfda.rxcui | |
| spl id | 0c441a11-2c3b-c0ef-e063-6294a90abc86 | id | |
| spl set id | aa694e0d-7891-4870-8106-dd57f1e29fb4 | 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.