warnings
Warnings For external use only ■ Avoid contact with eyes ■ If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.
Dr. Scholls Blister Pain Relief Complete Kit
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
- Dr. Scholls Blister Pain Relief Complete Kit
- Generic name
- LIDOCAINE
- Manufacturer
- Scholl's Wellness Company LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 58c2b35c-e1ed-7ea8-e063-6294a90a1494
- SPL ID
- 59618d9b-d3af-b795-e063-6294a90a7d93
- Version
- 2
- Effective date
- 2026-08-19
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:29
| 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 | Dr. Scholls Blister Pain Relief Complete Kit | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Scholl's Wellness Company LLC | openfda.manufacturer_name | |
| ndc | package | 73557-037-01 | openfda.package_ndc |
| ndc | package | 73469-0486-2 | openfda.package_ndc |
| ndc | product | 73469-0486 | openfda.product_ndc |
| ndc11 | package | 73469048602 | derived:openfda.package_ndc |
| ndc11 | package | 73557003701 | derived:openfda.package_ndc |
| rxcui | 1737778 | openfda.rxcui | |
| spl id | 59618d9b-d3af-b795-e063-6294a90a7d93 | id | |
| spl set id | 58c2b35c-e1ed-7ea8-e063-6294a90a1494 | set_id |
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.