warnings
Warnings For external use only.
SupreH 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
- SupreH Corn Remover Pads
- Generic name
- CORN REMOVER PADS
- Manufacturer
- Shenzhen Xinxin Yunhai Technology Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4e355fd3-cd42-eac3-e063-6294a90a2041
- SPL ID
- 4e355fd3-cd43-eac3-e063-6294a90a2041
- Version
- 1
- Effective date
- 2026-03-29
- Source export date
- 2026-09-24
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-24/9fd78a2f9f414685c74d5887a7cb123d3034b058c0efa372947847a4a10d3168/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 06858c06eb1cc3ec877527687035c43ee5d12c4c0df038a164bf6d5d4ba5dd73
- Import run
- 20260925T050722Z
- Imported at
- 2026-09-25 06:10:47
| 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 | SupreH Corn Remover Pads | openfda.brand_name | |
| generic name | CORN REMOVER PADS | openfda.generic_name | |
| manufacturer name | Shenzhen Xinxin Yunhai Technology Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 83818-032-01 | openfda.package_ndc |
| ndc | product | 83818-032 | openfda.product_ndc |
| ndc11 | package | 83818003201 | derived:openfda.package_ndc |
| rxcui | 240559 | openfda.rxcui | |
| spl id | 4e355fd3-cd43-eac3-e063-6294a90a2041 | id | |
| spl set id | 4e355fd3-cd42-eac3-e063-6294a90a2041 | 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.