warnings
Warnings
ANTACID Ultra Strength
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
- ANTACID Ultra Strength
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- CARDINAL HEALTH 110, LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d267ca31-09bd-46d3-be08-a259642f1b7f
- SPL ID
- 411d7abc-9cd4-0480-e063-6394a90a8bb8
- Version
- 3
- Effective date
- 2025-10-14
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:17
| 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 | ANTACID Ultra Strength | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | CARDINAL HEALTH 110, LLC. | openfda.manufacturer_name | |
| ndc | package | 70000-0683-1 | openfda.package_ndc |
| ndc | product | 70000-0683 | openfda.product_ndc |
| ndc11 | package | 70000068301 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | 411d7abc-9cd4-0480-e063-6394a90a8bb8 | id | |
| spl set id | d267ca31-09bd-46d3-be08-a259642f1b7f | 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.