warnings
WARNINGS Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Loratadine
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
- Loratadine
- Generic name
- LORATADINE
- Manufacturer
- MARKSANS PHARMA LIMITED
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c30907f9-1761-41e5-bd4e-2613e756e1c6
- SPL ID
- adf6c78c-edb1-4ffb-a934-d8cb772e621f
- Version
- 3
- Effective date
- 2021-11-15
- Source export date
- 2026-10-12
- 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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:46:17
| 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 | 206214 | derived:openfda.application_number |
| application number | ANDA206214 | openfda.application_number | |
| brand name | Loratadine | openfda.brand_name | |
| generic name | LORATADINE | openfda.generic_name | |
| manufacturer name | MARKSANS PHARMA LIMITED | openfda.manufacturer_name | |
| ndc | package | 25000-021-46 | openfda.package_ndc |
| ndc | package | 25000-021-34 | openfda.package_ndc |
| ndc | package | 25000-021-13 | openfda.package_ndc |
| ndc | package | 25000-021-08 | openfda.package_ndc |
| ndc | package | 25000-021-36 | openfda.package_ndc |
| ndc | package | 25000-021-21 | openfda.package_ndc |
| ndc | product | 25000-021 | openfda.product_ndc |
| ndc11 | package | 25000002108 | derived:openfda.package_ndc |
| ndc11 | package | 25000002146 | derived:openfda.package_ndc |
| ndc11 | package | 25000002121 | derived:openfda.package_ndc |
| ndc11 | package | 25000002136 | derived:openfda.package_ndc |
| ndc11 | package | 25000002134 | derived:openfda.package_ndc |
| ndc11 | package | 25000002113 | derived:openfda.package_ndc |
| rxcui | 828269 | openfda.rxcui | |
| spl id | adf6c78c-edb1-4ffb-a934-d8cb772e621f | id | |
| spl set id | c30907f9-1761-41e5-bd4e-2613e756e1c6 | set_id | |
| unii | 7AJO3BO7QN | 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.