warnings
Warnings Sore throat warning: severe or persistent sore throat for more than 2 days or if accompanied by a high fever, headache, nausea, vomiting, or rash may be serious. Consult a physician promptly.
Umcka Menthol
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
- Umcka Menthol
- Generic name
- PELARGONIUM SIDOIDES
- Manufacturer
- Schwabe North America, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a3d94c70-3d62-44a8-bdae-39b07e8e0e36
- SPL ID
- 85ee5b28-643c-448d-ad9e-961f27b2622e
- Version
- 12
- Effective date
- 2025-11-24
- Source export date
- 2026-10-12
- 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/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:27:03
| 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 |
|---|---|---|---|
| brand name | Umcka Menthol | openfda.brand_name | |
| generic name | PELARGONIUM SIDOIDES | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc | openfda.manufacturer_name | |
| ndc | package | 53499-5272-9 | openfda.package_ndc |
| ndc | package | 53499-5272-5 | openfda.package_ndc |
| ndc | product | 53499-5272 | openfda.product_ndc |
| ndc11 | package | 53499527209 | derived:openfda.package_ndc |
| ndc11 | package | 53499527205 | derived:openfda.package_ndc |
| spl id | 85ee5b28-643c-448d-ad9e-961f27b2622e | id | |
| spl set id | a3d94c70-3d62-44a8-bdae-39b07e8e0e36 | set_id | |
| unii | H6J53HEX8E | 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.