warnings
WARNINGS .
Goodsense 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
- Goodsense Ultra Strength Antacid
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 492deace-7ea1-4fe3-a4c7-b2c6f195d68c
- SPL ID
- 2aad8357-9bc4-4c30-aa82-51bfd9aff812
- Version
- 2
- Effective date
- 2025-01-20
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:17
| 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 | Goodsense Ultra Strength Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | Good Sense (Geiss, Destin & Dunn, Inc.) | openfda.manufacturer_name | |
| ndc | package | 50804-175-68 | openfda.package_ndc |
| ndc | product | 50804-175 | openfda.product_ndc |
| ndc11 | package | 50804017568 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | 2aad8357-9bc4-4c30-aa82-51bfd9aff812 | id | |
| spl set id | 492deace-7ea1-4fe3-a4c7-b2c6f195d68c | 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.