warnings
Warnings For external use only Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.
Coralite Pain 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
- Coralite Pain Relief
- Generic name
- CAMPHOR, MENTHOL, METHYL SALICYLATE
- Manufacturer
- United Exchange Corp.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 69aec845-3d4c-d226-e053-2991aa0afd12
- SPL ID
- 41b49d77-4471-c6ae-e063-6394a90aaac6
- Version
- 10
- Effective date
- 2025-10-21
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:43
| 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 | Coralite Pain Relief | openfda.brand_name | |
| generic name | CAMPHOR, MENTHOL, METHYL SALICYLATE | openfda.generic_name | |
| manufacturer name | United Exchange Corp. | openfda.manufacturer_name | |
| ndc | package | 65923-564-20 | openfda.package_ndc |
| ndc | product | 65923-564 | openfda.product_ndc |
| ndc11 | package | 65923056420 | derived:openfda.package_ndc |
| rxcui | 853260 | openfda.rxcui | |
| spl id | 41b49d77-4471-c6ae-e063-6394a90aaac6 | id | |
| spl set id | 69aec845-3d4c-d226-e053-2991aa0afd12 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii | |
| unii | LAV5U5022Y | 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.