warnings
Warnings Sore throat warnings: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.
COOL RELIEF ORAL ANESTHETIC
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
- COOL RELIEF ORAL ANESTHETIC
- Generic name
- MENTHOL
- Manufacturer
- Ricola USA Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3f93919f-e63e-470d-9d9a-f6ea3492c23d
- SPL ID
- cc708429-515c-421d-85da-07bc4c22a9ab
- Version
- 5
- Effective date
- 2024-12-10
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:24:33
| 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 number | M022 | openfda.application_number | |
| brand name | COOL RELIEF ORAL ANESTHETIC | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Ricola USA Inc. | openfda.manufacturer_name | |
| ndc | package | 63667-153-24 | openfda.package_ndc |
| ndc | package | 63667-153-19 | openfda.package_ndc |
| ndc | package | 63667-153-45 | openfda.package_ndc |
| ndc | product | 63667-153 | openfda.product_ndc |
| ndc11 | package | 63667015319 | derived:openfda.package_ndc |
| ndc11 | package | 63667015324 | derived:openfda.package_ndc |
| ndc11 | package | 63667015345 | derived:openfda.package_ndc |
| spl id | cc708429-515c-421d-85da-07bc4c22a9ab | id | |
| spl set id | 3f93919f-e63e-470d-9d9a-f6ea3492c23d | set_id | |
| unii | L7T10EIP3A | 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.