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WARNINGS For External Use Only.
Meijer Large Cold-Hot Medicated Patches
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
- Meijer Large Cold-Hot Medicated Patches
- Generic name
- MENTHOL
- Manufacturer
- Meijer Distribution Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- af0e7609-c320-414a-9df6-dfb3b08c8b82
- SPL ID
- 299259e9-21db-e0d2-e063-6394a90aa4d8
- Version
- 7
- Effective date
- 2024-12-18
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:24:38
| 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 | Meijer Large Cold-Hot Medicated Patches | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Meijer Distribution Inc | openfda.manufacturer_name | |
| ndc | package | 41250-834-05 | openfda.package_ndc |
| ndc | product | 41250-834 | openfda.product_ndc |
| ndc11 | package | 41250083405 | derived:openfda.package_ndc |
| rxcui | 420222 | openfda.rxcui | |
| spl id | 299259e9-21db-e0d2-e063-6394a90aa4d8 | id | |
| spl set id | af0e7609-c320-414a-9df6-dfb3b08c8b82 | 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.