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.
DUAL ACTION GLACIER MINT COUGH SUPPRESSANT 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
- DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC
- Generic name
- MENTHOL
- Manufacturer
- Ricola USA Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- db2ab9be-507d-4768-9d00-188f751b7726
- SPL ID
- fdd9887a-22ba-4242-9c08-77f202dc6973
- Version
- 4
- Effective date
- 2024-12-10
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:44:12
| 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 | M012 | openfda.application_number | |
| brand name | DUAL ACTION GLACIER MINT COUGH SUPPRESSANT ORAL ANESTHETIC | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Ricola USA Inc. | openfda.manufacturer_name | |
| ndc | package | 63667-603-19 | openfda.package_ndc |
| ndc | package | 63667-603-26 | openfda.package_ndc |
| ndc | product | 63667-603 | openfda.product_ndc |
| ndc11 | package | 63667060326 | derived:openfda.package_ndc |
| ndc11 | package | 63667060319 | derived:openfda.package_ndc |
| rxcui | 1424614 | openfda.rxcui | |
| spl id | fdd9887a-22ba-4242-9c08-77f202dc6973 | id | |
| spl set id | db2ab9be-507d-4768-9d00-188f751b7726 | 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.