warnings
Warnings For external use only
Boogie Hands Antibacterial Wet 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
- Boogie Hands Antibacterial Wet Wipes
- Generic name
- BENZALKONIUM CHLORIDE (0.13%)
- Manufacturer
- ELEEO BRANDS LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4009eb93-cef6-a202-e063-6394a90ae61b
- SPL ID
- 4009ebb1-142a-64a8-e063-6294a90a7555
- Version
- 1
- Effective date
- 2025-09-30
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:46:11
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Boogie Hands Antibacterial Wet Wipes | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE (0.13%) | openfda.generic_name | |
| manufacturer name | ELEEO BRANDS LLC | openfda.manufacturer_name | |
| ndc | package | 79747-014-02 | openfda.package_ndc |
| ndc | package | 79747-014-80 | openfda.package_ndc |
| ndc | package | 79747-014-30 | openfda.package_ndc |
| ndc | package | 79747-014-40 | openfda.package_ndc |
| ndc | package | 79747-014-20 | openfda.package_ndc |
| ndc | product | 79747-014 | openfda.product_ndc |
| ndc11 | package | 79747001402 | derived:openfda.package_ndc |
| ndc11 | package | 79747001480 | derived:openfda.package_ndc |
| ndc11 | package | 79747001430 | derived:openfda.package_ndc |
| ndc11 | package | 79747001420 | derived:openfda.package_ndc |
| ndc11 | package | 79747001440 | derived:openfda.package_ndc |
| spl id | 4009ebb1-142a-64a8-e063-6294a90a7555 | id | |
| spl set id | 4009eb93-cef6-a202-e063-6394a90ae61b | 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.