warnings
WARNINGS Do not take more than 18 teaspoonfuls in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.
Supreme Antacid Cherry
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
- Supreme Antacid Cherry
- Generic name
- CALCIUM CARBONATE, MAGNESIUM HYDROXIDE
- Manufacturer
- CVS
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2bc4ad16-57a1-b585-e063-6394a90a5726
- SPL ID
- 2107f543-71e7-4c2a-9e02-1632109e1013
- Version
- 3
- Effective date
- 2026-05-07
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:39:26
| 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 | Supreme Antacid Cherry | openfda.brand_name | |
| generic name | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | openfda.generic_name | |
| manufacturer name | CVS | openfda.manufacturer_name | |
| ndc | package | 51316-515-05 | openfda.package_ndc |
| ndc | product | 51316-515 | openfda.product_ndc |
| ndc11 | package | 51316051505 | derived:openfda.package_ndc |
| rxcui | 237865 | openfda.rxcui | |
| spl id | 2107f543-71e7-4c2a-9e02-1632109e1013 | id | |
| spl set id | 2bc4ad16-57a1-b585-e063-6394a90a5726 | set_id | |
| unii | NBZ3QY004S | openfda.unii | |
| unii | H0G9379FGK | 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.