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.
Menthol 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
- Menthol Cough Drops
- Generic name
- MENTHOL COUGH DROPS
- Manufacturer
- WHOLE FOODS MARKET, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1eb8927b-22c5-2ca3-e063-6294a90aa563
- SPL ID
- 1eb88fee-a9d5-a1f3-e063-6394a90aa631
- Version
- 1
- Effective date
- 2024-08-02
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:03:57
| 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 | Menthol Cough Drops | openfda.brand_name | |
| generic name | MENTHOL COUGH DROPS | openfda.generic_name | |
| manufacturer name | WHOLE FOODS MARKET, INC. | openfda.manufacturer_name | |
| ndc | package | 42681-0040-1 | openfda.package_ndc |
| ndc | product | 42681-0040 | openfda.product_ndc |
| ndc11 | package | 42681004001 | derived:openfda.package_ndc |
| rxcui | 476973 | openfda.rxcui | |
| spl id | 1eb88fee-a9d5-a1f3-e063-6394a90aa631 | id | |
| spl set id | 1eb8927b-22c5-2ca3-e063-6294a90aa563 | 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.