warnings
WARNINGS .
Ultra Strength Assorted Fruit 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 Assorted Fruit Antacid
- Generic name
- CALCIUM CARBONATE
- Manufacturer
- Hyvee Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 44eaa023-0f11-1256-e063-6394a90a4167
- SPL ID
- 1b9efee7-3f3f-410c-8308-213068644f6e
- Version
- 2
- Effective date
- 2026-03-26
- Source export date
- 2026-11-06
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:53:28
| 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 Assorted Fruit Antacid | openfda.brand_name | |
| generic name | CALCIUM CARBONATE | openfda.generic_name | |
| manufacturer name | Hyvee Inc | openfda.manufacturer_name | |
| ndc | package | 42507-709-68 | openfda.package_ndc |
| ndc | product | 42507-709 | openfda.product_ndc |
| ndc11 | package | 42507070968 | derived:openfda.package_ndc |
| rxcui | 308892 | openfda.rxcui | |
| spl id | 1b9efee7-3f3f-410c-8308-213068644f6e | id | |
| spl set id | 44eaa023-0f11-1256-e063-6394a90a4167 | 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.