warnings
Warnings
AMAZON 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
- AMAZON ULTRA STRENGTH ANTACID
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- AMAZON.COM SERVICES LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 36cf072c-ab61-47de-8fbc-f1d1d981ec84
- SPL ID
- 36cf072c-ab61-47de-8fbc-f1d1d981ec84
- Version
- 1
- Effective date
- 2026-03-27
- Source export date
- 2026-10-22
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-22/63b92dadbf6487b575e111b437d26dfb89c1d6401bf1507c742074f4503ba64d/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
- Import run
- 20261023T001338Z
- Imported at
- 2026-10-23 00:19:19
| 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 | AMAZON ULTRA STRENGTH ANTACID | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | AMAZON.COM SERVICES LLC | openfda.manufacturer_name | |
| ndc | package | 72288-504-60 | openfda.package_ndc |
| ndc | product | 72288-504 | openfda.product_ndc |
| ndc11 | package | 72288050460 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | 36cf072c-ab61-47de-8fbc-f1d1d981ec84 | id | |
| spl set id | 36cf072c-ab61-47de-8fbc-f1d1d981ec84 | 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.