warnings
Warnings: If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.
Tinnitus 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
- Tinnitus Relief
- Generic name
- CINCHONA OFFICINALIS BARK,SALICYLIC ACID,QUININE SULFATE,FERRUM PHOSPHORICUM,POTASSIUM CHLORIDE,CALOMEL,ALLYLTHIOUREA,.
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 30d67273-b9ec-4f3e-ace6-87a68325aaf1
- SPL ID
- 82fbfc25-3f57-460f-e053-2991aa0aad29
- Version
- 2
- Effective date
- 2019-02-28
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:48:09
| Harmonized routes |
|---|
| SUBLINGUAL |
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 | Tinnitus Relief | openfda.brand_name | |
| generic name | CINCHONA OFFICINALIS BARK,SALICYLIC ACID,QUININE SULFATE,FERRUM PHOSPHORICUM,POTASSIUM CHLORIDE,CALOMEL,ALLYLTHIOUREA,. | openfda.generic_name | |
| manufacturer name | Homeocare Laboratories | openfda.manufacturer_name | |
| ndc | package | 61727-315-21 | openfda.package_ndc |
| ndc | product | 61727-315 | openfda.product_ndc |
| ndc11 | package | 61727031521 | derived:openfda.package_ndc |
| spl id | 82fbfc25-3f57-460f-e053-2991aa0aad29 | id | |
| spl set id | 30d67273-b9ec-4f3e-ace6-87a68325aaf1 | set_id | |
| unii | J2D46N657D | openfda.unii | |
| unii | O414PZ4LPZ | openfda.unii | |
| unii | 91GQH8I5F7 | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | S003A158SB | openfda.unii | |
| unii | 706IDJ14B7 | openfda.unii | |
| unii | KF7Z0E0Q2B | 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.