warnings
Warnings For external use only.
Jointiva
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
- Jointiva
- Generic name
- TROLAMINE SALICYLATE 10%
- Manufacturer
- Rising Pharma Holdings, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3ee33cbf-7c0f-4982-b0b6-eeeb0202803b
- SPL ID
- efad21ab-3749-4ff3-8733-ff5c92ac621c
- Version
- 1
- Effective date
- 2025-12-11
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:47:23
| 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 | Jointiva | openfda.brand_name | |
| generic name | TROLAMINE SALICYLATE 10% | openfda.generic_name | |
| manufacturer name | Rising Pharma Holdings, Inc. | openfda.manufacturer_name | |
| ndc | package | 57237-355-85 | openfda.package_ndc |
| ndc | product | 57237-355 | openfda.product_ndc |
| ndc11 | package | 57237035585 | derived:openfda.package_ndc |
| rxcui | 313518 | openfda.rxcui | |
| spl id | efad21ab-3749-4ff3-8733-ff5c92ac621c | id | |
| spl set id | 3ee33cbf-7c0f-4982-b0b6-eeeb0202803b | set_id | |
| unii | H8O4040BHD | 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.