warnings
For external use only, Stop use and consult doctor if skin irritation develops.
Hand wipes
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
- Hand wipes
- Generic name
- HAND WIPES
- Manufacturer
- SHENZHEN BENLIJU BIO-TECH CO.,LTD
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 39f3acca-7275-88ca-e063-6394a90ad1a2
- SPL ID
- 479e6641-94d4-aac4-e063-6294a90a71b3
- Version
- 2
- Effective date
- 2026-01-05
- 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 05:14:54
| 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 | M003 | openfda.application_number | |
| brand name | Hand wipes | openfda.brand_name | |
| generic name | HAND WIPES | openfda.generic_name | |
| manufacturer name | SHENZHEN BENLIJU BIO-TECH CO.,LTD | openfda.manufacturer_name | |
| ndc | package | 84449-008-01 | openfda.package_ndc |
| ndc | product | 84449-008 | openfda.product_ndc |
| ndc11 | package | 84449000801 | derived:openfda.package_ndc |
| spl id | 479e6641-94d4-aac4-e063-6294a90a71b3 | id | |
| spl set id | 39f3acca-7275-88ca-e063-6394a90ad1a2 | set_id | |
| unii | F5UM2KM3W7 | 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.