warnings
Warnings For external use only.
Corn remover pads
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
- Corn remover pads
- Generic name
- CORN REMOVER PADS
- Manufacturer
- Henan Shouerkang Health Industry Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2e617119-531d-af7b-e063-6294a90a8ca6
- SPL ID
- 2e617123-2df7-68f1-e063-6294a90a2c90
- Version
- 1
- Effective date
- 2025-02-17
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:37:07
| Harmonized routes |
|---|
| CUTANEOUS |
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 | 505G(a)(3) | openfda.application_number | |
| brand name | Corn remover pads | openfda.brand_name | |
| generic name | CORN REMOVER PADS | openfda.generic_name | |
| manufacturer name | Henan Shouerkang Health Industry Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 85056-002-08 | openfda.package_ndc |
| ndc | package | 85056-002-07 | openfda.package_ndc |
| ndc | package | 85056-002-10 | openfda.package_ndc |
| ndc | package | 85056-002-06 | openfda.package_ndc |
| ndc | package | 85056-002-05 | openfda.package_ndc |
| ndc | package | 85056-002-09 | openfda.package_ndc |
| ndc | package | 85056-002-04 | openfda.package_ndc |
| ndc | package | 85056-002-02 | openfda.package_ndc |
| ndc | package | 85056-002-01 | openfda.package_ndc |
| ndc | package | 85056-002-03 | openfda.package_ndc |
| ndc | product | 85056-002 | openfda.product_ndc |
| ndc11 | package | 85056000201 | derived:openfda.package_ndc |
| ndc11 | package | 85056000210 | derived:openfda.package_ndc |
| ndc11 | package | 85056000206 | derived:openfda.package_ndc |
| ndc11 | package | 85056000208 | derived:openfda.package_ndc |
| ndc11 | package | 85056000205 | derived:openfda.package_ndc |
| ndc11 | package | 85056000202 | derived:openfda.package_ndc |
| ndc11 | package | 85056000209 | derived:openfda.package_ndc |
| ndc11 | package | 85056000207 | derived:openfda.package_ndc |
| ndc11 | package | 85056000203 | derived:openfda.package_ndc |
| ndc11 | package | 85056000204 | derived:openfda.package_ndc |
| spl id | 2e617123-2df7-68f1-e063-6294a90a2c90 | id | |
| spl set id | 2e617119-531d-af7b-e063-6294a90a8ca6 | 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.