warnings
Warnings Sore throat warning: severe or persistence sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.
Cough Drops
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
- Cough Drops
- Generic name
- MENTHOL
- Manufacturer
- Topco Associates LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- eff0b37b-6c08-b687-e053-2a95a90a11a9
- SPL ID
- 23e6ee3d-b4d9-3973-e063-6394a90a3e08
- Version
- 2
- Effective date
- 2024-10-07
- Source export date
- 2026-10-27
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:12:55
| 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 | Cough Drops | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Topco Associates LLC | openfda.manufacturer_name | |
| ndc | package | 76162-011-01 | openfda.package_ndc |
| ndc | product | 76162-011 | openfda.product_ndc |
| ndc11 | package | 76162001101 | derived:openfda.package_ndc |
| rxcui | 485287 | openfda.rxcui | |
| spl id | 23e6ee3d-b4d9-3973-e063-6394a90a3e08 | id | |
| spl set id | eff0b37b-6c08-b687-e053-2a95a90a11a9 | 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.