warnings
Warning For external use only
Scott Clear Corn Removers
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
- Scott Clear Corn Removers
- Generic name
- 40% W/W SALICYLIC ACID CORN REMOVER
- Manufacturer
- Creative Foam Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- dd949b90-2f11-75eb-e053-2995a90af5a5
- SPL ID
- 4539780a-cdb1-bbdc-e063-6394a90a3169
- Version
- 7
- Effective date
- 2025-12-05
- Source export date
- 2026-10-27
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:57:51
| 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 | M030 | openfda.application_number | |
| brand name | Scott Clear Corn Removers | openfda.brand_name | |
| generic name | 40% W/W SALICYLIC ACID CORN REMOVER | openfda.generic_name | |
| manufacturer name | Creative Foam Corporation | openfda.manufacturer_name | |
| ndc | package | 82660-006-05 | openfda.package_ndc |
| ndc | product | 82660-006 | openfda.product_ndc |
| ndc11 | package | 82660000605 | derived:openfda.package_ndc |
| rxcui | 240559 | openfda.rxcui | |
| spl id | 4539780a-cdb1-bbdc-e063-6394a90a3169 | id | |
| spl set id | dd949b90-2f11-75eb-e053-2995a90af5a5 | set_id | |
| unii | O414PZ4LPZ | 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.