warnings
WARNINGS .
Extra Strength Antacid Assorted Fruit
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
- Extra Strength Antacid Assorted Fruit
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- Hyvee Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4cda1c1a-f5ff-5b77-e063-6294a90ad664
- SPL ID
- 0688a639-0392-47a1-ba1f-ea2412dbebba
- Version
- 2
- Effective date
- 2026-05-13
- Source export date
- 2026-10-22
- 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/2026-10-22/14398cbe7e22245154b804e51e14ec487486e2bb68b514fde0d7c34660e837f0/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
- Import run
- 20261023T001338Z
- Imported at
- 2026-10-23 00:35:05
| 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 | Extra Strength Antacid Assorted Fruit | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | Hyvee Inc | openfda.manufacturer_name | |
| ndc | package | 42507-195-96 | openfda.package_ndc |
| ndc | product | 42507-195 | openfda.product_ndc |
| ndc11 | package | 42507019596 | derived:openfda.package_ndc |
| rxcui | 308915 | openfda.rxcui | |
| spl id | 0688a639-0392-47a1-ba1f-ea2412dbebba | id | |
| spl set id | 4cda1c1a-f5ff-5b77-e063-6294a90ad664 | set_id | |
| 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.