warnings
Warnings
Green Guard 24 Hour Allergy Relief
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
- Green Guard 24 Hour Allergy Relief
- Generic name
- LORATADINE
- Manufacturer
- Unifirst First Aid Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f98a45fd-cda8-4884-e053-6294a90a57b5
- SPL ID
- 441b212c-1a4f-5b61-e063-6294a90a63fd
- Version
- 5
- Effective date
- 2025-11-21
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:29:13
| 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 | 210722 | derived:openfda.application_number |
| application number | ANDA210722 | openfda.application_number | |
| brand name | Medi-First Plus Allery Relief | openfda.brand_name | |
| brand name | Medique Loradamed | openfda.brand_name | |
| brand name | Green Guard 24 Hour Allergy Relief | openfda.brand_name | |
| generic name | LORATADINE | openfda.generic_name | |
| manufacturer name | Unifirst First Aid Corporation | openfda.manufacturer_name | |
| ndc | package | 47682-403-12 | openfda.package_ndc |
| ndc | package | 47682-403-50 | openfda.package_ndc |
| ndc | package | 47682-117-46 | openfda.package_ndc |
| ndc | package | 47682-912-33 | openfda.package_ndc |
| ndc | package | 47682-117-50 | openfda.package_ndc |
| ndc | package | 47682-912-46 | openfda.package_ndc |
| ndc | package | 47682-403-46 | openfda.package_ndc |
| ndc | product | 47682-117 | openfda.product_ndc |
| ndc | product | 47682-403 | openfda.product_ndc |
| ndc | product | 47682-912 | openfda.product_ndc |
| ndc11 | package | 47682040346 | derived:openfda.package_ndc |
| ndc11 | package | 47682040350 | derived:openfda.package_ndc |
| ndc11 | package | 47682091233 | derived:openfda.package_ndc |
| ndc11 | package | 47682011746 | derived:openfda.package_ndc |
| ndc11 | package | 47682011750 | derived:openfda.package_ndc |
| ndc11 | package | 47682091246 | derived:openfda.package_ndc |
| ndc11 | package | 47682040312 | derived:openfda.package_ndc |
| rxcui | 311372 | openfda.rxcui | |
| spl id | 441b212c-1a4f-5b61-e063-6294a90a63fd | id | |
| spl set id | f98a45fd-cda8-4884-e053-6294a90a57b5 | 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.