warnings
Caution Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Directions Tear open packet, unfold and use as a washcloth.
BZK Towelette
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
- BZK Towelette
- Generic name
- BENZALKONIUM CHLORIDE
- Manufacturer
- Acme United Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 866fdc1e-19b2-4d79-e053-2a91aa0a36fe
- SPL ID
- 866f9e78-87a0-7919-e053-2a91aa0a4058
- Version
- 1
- Effective date
- 2019-04-16
- Source export date
- 2026-10-12
- 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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:54:25
| 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 | part333A | openfda.application_number | |
| brand name | BZK Towelette | openfda.brand_name | |
| generic name | BENZALKONIUM CHLORIDE | openfda.generic_name | |
| manufacturer name | Acme United Corporation | openfda.manufacturer_name | |
| ndc | package | 0924-7112-04 | openfda.package_ndc |
| ndc | package | 0924-7112-02 | openfda.package_ndc |
| ndc | package | 0924-7112-03 | openfda.package_ndc |
| ndc | package | 0924-7112-00 | openfda.package_ndc |
| ndc | package | 0924-7112-01 | openfda.package_ndc |
| ndc | package | 0924-7112-05 | openfda.package_ndc |
| ndc | product | 0924-7112 | openfda.product_ndc |
| ndc11 | package | 00924711202 | derived:openfda.package_ndc |
| ndc11 | package | 00924711205 | derived:openfda.package_ndc |
| ndc11 | package | 00924711201 | derived:openfda.package_ndc |
| ndc11 | package | 00924711203 | derived:openfda.package_ndc |
| ndc11 | package | 00924711204 | derived:openfda.package_ndc |
| ndc11 | package | 00924711200 | derived:openfda.package_ndc |
| rxcui | 1043307 | openfda.rxcui | |
| spl id | 866f9e78-87a0-7919-e053-2a91aa0a4058 | id | |
| spl set id | 866fdc1e-19b2-4d79-e053-2a91aa0a36fe | 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.