warnings
Warnings
Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
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
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 796c4b81-145b-4050-a851-dec81ff97006
- SPL ID
- a0bd1e9b-eb9f-46e7-8cee-10bde092d7cb
- Version
- 11
- Effective date
- 2024-11-27
- Source export date
- 2026-10-27
- 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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:53:10
| 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 | 090922 | derived:openfda.application_number |
| application number | ANDA090922 | openfda.application_number | |
| brand name | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | openfda.brand_name | |
| generic name | CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Sun Pharmaceutical Industries, Inc. | openfda.manufacturer_name | |
| ndc | package | 62756-915-60 | openfda.package_ndc |
| ndc | package | 62756-915-62 | openfda.package_ndc |
| ndc | package | 62756-915-73 | openfda.package_ndc |
| ndc | product | 62756-915 | openfda.product_ndc |
| ndc11 | package | 62756091562 | derived:openfda.package_ndc |
| ndc11 | package | 62756091560 | derived:openfda.package_ndc |
| ndc11 | package | 62756091573 | derived:openfda.package_ndc |
| rxcui | 1014571 | openfda.rxcui | |
| spl id | a0bd1e9b-eb9f-46e7-8cee-10bde092d7cb | id | |
| spl set id | 796c4b81-145b-4050-a851-dec81ff97006 | set_id | |
| unii | 64O047KTOA | openfda.unii | |
| unii | 6V9V2RYJ8N | 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.