YULAM DIE DA WAN HUA PAIN RELIEVING
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
- YULAM DIE DA WAN HUA PAIN RELIEVING
- Generic name
- MENTHOL AND CAMPHOR
- Manufacturer
- MADISON ONE ACME INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1ba3c31b-2737-4b55-a0ea-90013a1d8cf4
- SPL ID
- 436c7247-846c-a7ac-e063-6294a90a2c5b
- Version
- 3
- Effective date
- 2025-11-12
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:21
| 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 | YULAM DIE DA WAN HUA PAIN RELIEVING | openfda.brand_name | |
| generic name | MENTHOL AND CAMPHOR | openfda.generic_name | |
| manufacturer name | MADISON ONE ACME INC | openfda.manufacturer_name | |
| ndc | package | 55614-740-01 | openfda.package_ndc |
| ndc | product | 55614-740 | openfda.product_ndc |
| ndc11 | package | 55614074001 | derived:openfda.package_ndc |
| rxcui | 2619676 | openfda.rxcui | |
| spl id | 436c7247-846c-a7ac-e063-6294a90a2c5b | id | |
| spl set id | 1ba3c31b-2737-4b55-a0ea-90013a1d8cf4 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii |
Warnings cross-check#
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Warnings For external use only
Adverse reactions cross-check#
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adverse reactions
Report any unexpected side effects from the use of this product to the FDA MedWatch Program.
Reported adverse events (FAERS/openFDA)#
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