warnings
In case of accidental ingestion, get medical help or contact a Poison Control Center right away. Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Ring 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
- Ring Relief
- Generic name
- ARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, THIOSINAMINUM, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREA
- Manufacturer
- TRP Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1c9c7944-31a9-4019-aad5-6b7f86084b53
- SPL ID
- 46065bc3-19da-9699-e063-6394a90a386f
- Version
- 14
- Effective date
- 2025-12-15
- 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 06:18:12
| Harmonized routes |
|---|
| AURICULAR (OTIC) |
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 |
|---|---|---|---|
| brand name | Ring Relief | openfda.brand_name | |
| generic name | ARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, THIOSINAMINUM, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREA | openfda.generic_name | |
| manufacturer name | TRP Company | openfda.manufacturer_name | |
| ndc | package | 17312-001-11 | openfda.package_ndc |
| ndc | package | 17312-001-15 | openfda.package_ndc |
| ndc | product | 17312-001 | openfda.product_ndc |
| ndc11 | package | 17312000115 | derived:openfda.package_ndc |
| ndc11 | package | 17312000111 | derived:openfda.package_ndc |
| spl id | 46065bc3-19da-9699-e063-6394a90a386f | id | |
| spl set id | 1c9c7944-31a9-4019-aad5-6b7f86084b53 | set_id | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | 324Y4038G2 | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | O414PZ4LPZ | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 706IDJ14B7 | openfda.unii | |
| unii | C88X29Y479 | openfda.unii | |
| unii | 1MBW07J51Q | 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.