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WARNINGS For External Use Only.
Good Sense Hot and Cold Medicated Patch
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
- Good Sense Hot and Cold Medicated Patch
- Generic name
- MENTHOL
- Manufacturer
- GOOD SENSE
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e
- SPL ID
- 2995c547-8a92-6786-e063-6294a90a112b
- Version
- 10
- Effective date
- 2024-12-18
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:20
| Harmonized routes |
|---|
| TOPICAL |
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 | M017 | openfda.application_number | |
| brand name | Good Sense Hot and Cold Medicated Patch | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | GOOD SENSE | openfda.manufacturer_name | |
| ndc | package | 50804-124-13 | openfda.package_ndc |
| ndc | product | 50804-124 | openfda.product_ndc |
| ndc11 | package | 50804012413 | derived:openfda.package_ndc |
| rxcui | 420222 | openfda.rxcui | |
| spl id | 2995c547-8a92-6786-e063-6294a90a112b | id | |
| spl set id | 1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e | 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.