warnings
WARNINGS .
Regular Strength Antacid
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
- Regular Strength Antacid
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- DeMoulas Market Basket
- Product type
- HUMAN OTC DRUG
- SPL set ID
- be167e45-3db8-4739-91ac-e83d55223617
- SPL ID
- be167e45-3db8-4739-91ac-e83d55223617
- Version
- 1
- Effective date
- 2025-02-07
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:45:33
| 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 | Regular Strength Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | DeMoulas Market Basket | openfda.manufacturer_name | |
| ndc | package | 53942-126-17 | openfda.package_ndc |
| ndc | product | 53942-126 | openfda.product_ndc |
| ndc11 | package | 53942012617 | derived:openfda.package_ndc |
| rxcui | 308907 | openfda.rxcui | |
| spl id | be167e45-3db8-4739-91ac-e83d55223617 | id | |
| spl set id | be167e45-3db8-4739-91ac-e83d55223617 | 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.