warnings
Warnings Sore throat warning: 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.
COUGH DROPS- menthol granule
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- menthol granule
- Generic name
- MENTHOL GRANULE
- Manufacturer
- Anhui Jiuhe Health Industry Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5351b943-5830-e4e7-e063-6394a90a5b66
- SPL ID
- 563ee31a-f76d-339a-e063-6294a90acb3b
- Version
- 2
- Effective date
- 2026-07-10
- Source export date
- 2026-09-28
- 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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:50
| 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- menthol granule | openfda.brand_name | |
| generic name | MENTHOL GRANULE | openfda.generic_name | |
| manufacturer name | Anhui Jiuhe Health Industry Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 87745-002-07 | openfda.package_ndc |
| ndc | package | 87745-002-05 | openfda.package_ndc |
| ndc | package | 87745-002-03 | openfda.package_ndc |
| ndc | package | 87745-002-02 | openfda.package_ndc |
| ndc | package | 87745-002-08 | openfda.package_ndc |
| ndc | package | 87745-002-04 | openfda.package_ndc |
| ndc | package | 87745-002-01 | openfda.package_ndc |
| ndc | package | 87745-002-06 | openfda.package_ndc |
| ndc | product | 87745-002 | openfda.product_ndc |
| ndc11 | package | 87745000207 | derived:openfda.package_ndc |
| ndc11 | package | 87745000201 | derived:openfda.package_ndc |
| ndc11 | package | 87745000202 | derived:openfda.package_ndc |
| ndc11 | package | 87745000208 | derived:openfda.package_ndc |
| ndc11 | package | 87745000204 | derived:openfda.package_ndc |
| ndc11 | package | 87745000203 | derived:openfda.package_ndc |
| ndc11 | package | 87745000206 | derived:openfda.package_ndc |
| ndc11 | package | 87745000205 | derived:openfda.package_ndc |
| spl id | 563ee31a-f76d-339a-e063-6294a90acb3b | id | |
| spl set id | 5351b943-5830-e4e7-e063-6394a90a5b66 | 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.