warnings
Warnings For external use only Allergy alert: This product contains natural rubber latex which may cause allergic reactions
ARTHRITIS PAIN RELIEF
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
- ARTHRITIS PAIN RELIEF
- Generic name
- CAMPHOR, CAPSAICIN, METHYL SALICYLATE
- Manufacturer
- YUNNAN BAIYAO GROUP CO., LTD.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 671c57f0-3c6f-4416-bc81-f6930fef327b
- SPL ID
- 3a7a1fb4-c769-c4c7-e063-6394a90ab935
- Version
- 5
- Effective date
- 2025-07-21
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:58:16
| 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 | ARTHRITIS PAIN RELIEF | openfda.brand_name | |
| generic name | CAMPHOR, CAPSAICIN, METHYL SALICYLATE | openfda.generic_name | |
| manufacturer name | YUNNAN BAIYAO GROUP CO., LTD. | openfda.manufacturer_name | |
| ndc | package | 61658-002-01 | openfda.package_ndc |
| ndc | product | 61658-002 | openfda.product_ndc |
| ndc11 | package | 61658000201 | derived:openfda.package_ndc |
| spl id | 3a7a1fb4-c769-c4c7-e063-6394a90ab935 | id | |
| spl set id | 671c57f0-3c6f-4416-bc81-f6930fef327b | set_id | |
| unii | S07O44R1ZM | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii | |
| unii | LAV5U5022Y | 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.