warnings
For external use only
Sinsinpas Arex Pain Relieving Patch, Medium
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
- Sinsinpas Arex Pain Relieving Patch, Medium
- Generic name
- CAMPHOR, MENTHOL, METHYL SALICYLATE
- Manufacturer
- Sinsin Pharmaceutical Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 46453ef2-512b-4852-e063-6394a90a8912
- SPL ID
- 5a244916-b21e-857b-e063-6394a90aeb48
- Version
- 4
- Effective date
- 2026-08-28
- Source export date
- 2026-10-30
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:30:08
| Harmonized routes |
|---|
| CUTANEOUS, TOPICAL, TRANSDERMAL |
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 | Sinsinpas Arex Pain Relieving Patch, Medium | openfda.brand_name | |
| generic name | CAMPHOR, MENTHOL, METHYL SALICYLATE | openfda.generic_name | |
| manufacturer name | Sinsin Pharmaceutical Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 55264-022-11 | openfda.package_ndc |
| ndc | product | 55264-022 | openfda.product_ndc |
| ndc11 | package | 55264002211 | derived:openfda.package_ndc |
| rxcui | 2730670 | openfda.rxcui | |
| spl id | 5a244916-b21e-857b-e063-6394a90aeb48 | id | |
| spl set id | 46453ef2-512b-4852-e063-6394a90a8912 | set_id | |
| unii | 5TJD82A1ET | openfda.unii | |
| unii | BZ1R15MTK7 | openfda.unii | |
| unii | LAV5U5022Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings and cautions
This product contains natural rubber which may cause allergic reactions.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.