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 way.
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
- INNOVUS PHARMACEUTICALS, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a4e92bd2-8f75-4acc-9b75-df8332bd4cc4
- SPL ID
- 72b23ff2-70a3-412c-9a9c-902927598e2f
- Version
- 3
- Effective date
- 2026-06-04
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/5ab46f90f6b44e2aa9affb3cb9a1420d82b92a8f942c23fe463364760a659d66/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:09:17
| 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 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 | INNOVUS PHARMACEUTICALS, INC. | openfda.manufacturer_name | |
| ndc | package | 57483-120-42 | openfda.package_ndc |
| ndc | package | 57483-120-14 | openfda.package_ndc |
| ndc | product | 57483-120 | openfda.product_ndc |
| ndc11 | package | 57483012042 | derived:openfda.package_ndc |
| ndc11 | package | 57483012014 | derived:openfda.package_ndc |
| rxcui | 402014 | openfda.rxcui | |
| spl id | 72b23ff2-70a3-412c-9a9c-902927598e2f | id | |
| spl set id | a4e92bd2-8f75-4acc-9b75-df8332bd4cc4 | 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.