warnings
Warnings Allergy alert: Do not use if you are allergic to omeprazole
Acid Reducer
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
- Acid Reducer
- Generic name
- OMEPRAZOLE
- Manufacturer
- Aurohealth LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3eb70031-6439-44cf-8056-3e2e1e4a7fa9
- SPL ID
- d4d5397d-41ee-4c3c-bf0f-a923b1731d0b
- Version
- 7
- Effective date
- 2024-06-27
- Source export date
- 2026-09-28
- 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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:11
| 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 applno | ANDA | 206877 | derived:openfda.application_number |
| application number | ANDA206877 | openfda.application_number | |
| brand name | Acid Reducer | openfda.brand_name | |
| generic name | OMEPRAZOLE | openfda.generic_name | |
| manufacturer name | Aurohealth LLC | openfda.manufacturer_name | |
| ndc | package | 58602-826-05 | openfda.package_ndc |
| ndc | package | 58602-826-62 | openfda.package_ndc |
| ndc | package | 58602-826-61 | openfda.package_ndc |
| ndc | product | 58602-826 | openfda.product_ndc |
| ndc11 | package | 58602082662 | derived:openfda.package_ndc |
| ndc11 | package | 58602082605 | derived:openfda.package_ndc |
| ndc11 | package | 58602082661 | derived:openfda.package_ndc |
| rxcui | 402014 | openfda.rxcui | |
| spl id | d4d5397d-41ee-4c3c-bf0f-a923b1731d0b | id | |
| spl set id | 3eb70031-6439-44cf-8056-3e2e1e4a7fa9 | set_id | |
| unii | 426QFE7XLK | 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.