warnings
Warnings: A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur.
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 - MERCURIUS SOLUBILIS - SALICYLIC ACID - SILICON DIOXIDE - ALLYLTHIOUREA -
- Manufacturer
- TRP Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- aa2cd967-3c27-4afe-8751-7ea50ab62913
- SPL ID
- 4606551b-3bef-8c1b-e063-6394a90a0160
- Version
- 13
- Effective date
- 2025-12-15
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:34
| Harmonized routes |
|---|
| ORAL |
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 - MERCURIUS SOLUBILIS - SALICYLIC ACID - SILICON DIOXIDE - ALLYLTHIOUREA - | openfda.generic_name | |
| manufacturer name | TRP Company | openfda.manufacturer_name | |
| ndc | package | 17312-023-14 | openfda.package_ndc |
| ndc | product | 17312-023 | openfda.product_ndc |
| ndc11 | package | 17312002314 | derived:openfda.package_ndc |
| spl id | 4606551b-3bef-8c1b-e063-6394a90a0160 | id | |
| spl set id | aa2cd967-3c27-4afe-8751-7ea50ab62913 | 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.
warnings
In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if: You experience ear pain or worsening symptoms. Symptoms last longer than 7 days.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.