warnings
Warnings
Ultra Strength Natural 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 Natural Antacid
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- KROGER COMPANY
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2931d427-b2be-4db9-a58d-ff89c221ff51
- SPL ID
- a8f71246-d08f-4b88-8a39-f19f0ce090b4
- Version
- 8
- Effective date
- 2026-08-31
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:15:39
| 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 Natural Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | KROGER COMPANY | openfda.manufacturer_name | |
| ndc | package | 30142-108-72 | openfda.package_ndc |
| ndc | product | 30142-108 | openfda.product_ndc |
| ndc11 | package | 30142010872 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | a8f71246-d08f-4b88-8a39-f19f0ce090b4 | id | |
| spl set id | 2931d427-b2be-4db9-a58d-ff89c221ff51 | 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.