warnings
Warnings
AREX SINSIN PAS
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
- AREX SINSIN PAS
- Generic name
- CAMPHOR, MENTHA OIL, MENTHOL, METHYL SALICYLATE, ZINC OXIDE
- Manufacturer
- Sinsin Pharmaceutical Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2013ea44-e2ea-4b36-bddb-7f64163284b6
- SPL ID
- 409672cd-3303-b2e0-e063-6294a90a3569
- Version
- 10
- Effective date
- 2025-10-07
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:09
| 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 | AREX SINSIN PAS | openfda.brand_name | |
| generic name | CAMPHOR, MENTHA OIL, MENTHOL, METHYL SALICYLATE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | Sinsin Pharmaceutical Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 55264-020-10 | openfda.package_ndc |
| ndc | product | 55264-020 | openfda.product_ndc |
| ndc11 | package | 55264002010 | derived:openfda.package_ndc |
| spl id | 409672cd-3303-b2e0-e063-6294a90a3569 | id | |
| spl set id | 2013ea44-e2ea-4b36-bddb-7f64163284b6 | set_id | |
| unii | AV092KU4JH | openfda.unii | |
| unii | SOI2LOH54Z | openfda.unii | |
| 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
For external use only.
warnings
Do not use on wounds or damaged skin if you are allergic to aspirin or salicylates with a heating pad with, or at the same time as, other external analgesic products. Ask a doctor before use if you are allergic to any ingredients of this product When using this product do not use otherwise than directed. avoid contact with the eyes, mucous membranes or rashes. Stop use and ask a doctor if rash, itching or excessive skin irritation develops. conditions worsen. symptoms persist for more than 7 days. symptoms clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
warnings and cautions
Caution: This product contains natural rubber latex which may cause allergic reactions.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.