warnings
WARNINGS .
Ultra Strength Antacid Assorted Berries
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 Assorted Berries
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- Guardian Drug Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7f0ca229-7452-4f18-bd2f-bf2dfc3482f8
- SPL ID
- 7f0ca229-7452-4f18-bd2f-bf2dfc3482f8
- Version
- 1
- Effective date
- 2025-02-06
- Source export date
- 2026-10-27
- 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/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:22:47
| 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 Assorted Berries | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | Guardian Drug Company | openfda.manufacturer_name | |
| ndc | package | 53041-161-68 | openfda.package_ndc |
| ndc | product | 53041-161 | openfda.product_ndc |
| ndc11 | package | 53041016168 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | 7f0ca229-7452-4f18-bd2f-bf2dfc3482f8 | id | |
| spl set id | 7f0ca229-7452-4f18-bd2f-bf2dfc3482f8 | 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.