warnings
Warnings Allergy alert: Do not use if you are allergic to omeprazole. Omeprazole may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If an allergic reaction occurs, stop use and seek medical help right away.
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
- Family Dollar Stores, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6d8daf78-1672-4bbf-a022-514bf0a5ac9a
- SPL ID
- c1eee169-a04a-485d-9c17-2229cdca1fd1
- Version
- 8
- Effective date
- 2024-06-17
- 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 05:20:53
| 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 | Family Dollar Stores, LLC | openfda.manufacturer_name | |
| ndc | package | 55319-037-05 | openfda.package_ndc |
| ndc | package | 55319-037-62 | openfda.package_ndc |
| ndc | product | 55319-037 | openfda.product_ndc |
| ndc11 | package | 55319003762 | derived:openfda.package_ndc |
| ndc11 | package | 55319003705 | derived:openfda.package_ndc |
| rxcui | 402014 | openfda.rxcui | |
| spl id | c1eee169-a04a-485d-9c17-2229cdca1fd1 | id | |
| spl set id | 6d8daf78-1672-4bbf-a022-514bf0a5ac9a | 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.