FDA label 198666bb-d32d-48a5-9e1c-1bae898c4fac
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
- SPL set ID
- 394cd041-ab9d-4d25-aa42-b2ebbdfabec0
- SPL ID
- 198666bb-d32d-48a5-9e1c-1bae898c4fac
- Version
- 2
- Effective date
- 2011-06-23
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:42:01
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 |
|---|---|---|---|
| spl id | 198666bb-d32d-48a5-9e1c-1bae898c4fac | id | |
| spl set id | 394cd041-ab9d-4d25-aa42-b2ebbdfabec0 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5. WARNINGS AND PRECAUTIONS 5.1. Joint pain requires differential diagnosis for acute or subacute viral diseases, bacterial infection, pain due to overweight (leg joints) hyperuricemia syndrome, gout, and referred pain. 5.2. Patients with known sensitivity to salycilates should be monitored closely during the therapy, and should only be treated after successful application of a test dose without adverse effects. 5.3. Skin cleansing/disinfection is required before application. Saprophytic bacteria may produce injection site abscesses with improper skin preparation
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6. ADVERSE REACTIONS 6.1. The most common mild adverse reaction is slight reddening at the injection site due to the mechanical effect of the needle or a superficial skin reaction of mild erythema.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.