warnings
Warnings For external use only.
Quality Choice Lidocaine Pain Relief Patch
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
- Quality Choice Lidocaine Pain Relief Patch
- Generic name
- LIDOCAINE
- Manufacturer
- Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 526abe69-4bbc-6e73-e063-6394a90ad25d
- SPL ID
- 53c443fd-b817-72a7-e063-6394a90a5aa9
- Version
- 2
- Effective date
- 2026-06-08
- Source export date
- 2026-11-06
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/8ec9b1418c25a8bb472a36e6bc0b2cbabb210d48d5dd734197e022d21529ed58/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 09:17:08
| 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 | Quality Choice Lidocaine Pain Relief Patch | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) | openfda.manufacturer_name | |
| ndc | package | 83324-257-05 | openfda.package_ndc |
| ndc | product | 83324-257 | openfda.product_ndc |
| ndc11 | package | 83324025705 | derived:openfda.package_ndc |
| rxcui | 1737778 | openfda.rxcui | |
| spl id | 53c443fd-b817-72a7-e063-6394a90a5aa9 | id | |
| spl set id | 526abe69-4bbc-6e73-e063-6394a90ad25d | set_id | |
| unii | 98PI200987 | 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.