warnings
WARNINGS .
Ultra 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
- Ultra Strength Antacid
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- UNITED NATURAL FOODS, INC. DBA UNFI
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1cbea7c2-fdc0-5a6b-e063-6294a90a9cfa
- SPL ID
- a1148985-2ab1-4474-952c-732c05f5fd56
- Version
- 2
- Effective date
- 2025-02-07
- Source export date
- 2026-11-06
- 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/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:44:24
| 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 | Ultra Strength Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | UNITED NATURAL FOODS, INC. DBA UNFI | openfda.manufacturer_name | |
| ndc | package | 83455-171-68 | openfda.package_ndc |
| ndc | product | 83455-171 | openfda.product_ndc |
| ndc11 | package | 83455017168 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | a1148985-2ab1-4474-952c-732c05f5fd56 | id | |
| spl set id | 1cbea7c2-fdc0-5a6b-e063-6294a90a9cfa | 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.