warnings
Warnings Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or follow headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.
DISCOUNT DRUG MART
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
- DISCOUNT DRUG MART
- Generic name
- COUGH DROPS MENTHOL
- Manufacturer
- DISCOUNT DRUG MART
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 55656a74-9721-62cf-e063-6394a90a7eb7
- SPL ID
- 55657d1f-3a12-1d84-e063-6394a90abe1c
- Version
- 1
- Effective date
- 2026-06-29
- Source export date
- 2026-11-06
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:36:44
| 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 | DISCOUNT DRUG MART | openfda.brand_name | |
| generic name | COUGH DROPS MENTHOL | openfda.generic_name | |
| manufacturer name | DISCOUNT DRUG MART | openfda.manufacturer_name | |
| ndc | package | 53943-209-30 | openfda.package_ndc |
| ndc | product | 53943-209 | openfda.product_ndc |
| ndc11 | package | 53943020930 | derived:openfda.package_ndc |
| rxcui | 485287 | openfda.rxcui | |
| spl id | 55657d1f-3a12-1d84-e063-6394a90abe1c | id | |
| spl set id | 55656a74-9721-62cf-e063-6394a90a7eb7 | 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.