warnings
Warnings For external use only Allergy alert: This product may cause allergic reaction in some individuals. Test on small area before use.
Coralite Ultra Strength 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 Ultra Strength Pain Relief
- Generic name
- CAMPHOR MENTHOL
- Manufacturer
- United Exchange Corp.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 44ecf959-cc07-4adc-a500-075b2ee69548
- SPL ID
- 425530d6-e8ea-f05c-e063-6294a90aff39
- Version
- 13
- Effective date
- 2025-10-29
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:19
| 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 Ultra Strength Pain Relief | openfda.brand_name | |
| generic name | CAMPHOR MENTHOL | openfda.generic_name | |
| manufacturer name | United Exchange Corp. | openfda.manufacturer_name | |
| ndc | package | 65923-532-18 | openfda.package_ndc |
| ndc | product | 65923-532 | openfda.product_ndc |
| ndc11 | package | 65923053218 | derived:openfda.package_ndc |
| rxcui | 1089831 | openfda.rxcui | |
| spl id | 425530d6-e8ea-f05c-e063-6294a90aff39 | id | |
| spl set id | 44ecf959-cc07-4adc-a500-075b2ee69548 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | 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.