Indications and uses
First Aid to help reduce the risk of infection in minor cuts, scrapes and burns Updaed Indications & USage section to be in line with the OTC Monograph
BZK
- Manufacturer
- Henry Schein Inc.
- Effective date
- 2024-04-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 00:10:37
Label at a glance#
ProductBZK
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections
Dosage and administration
Tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping. Inactive ingredients purified water, alcohol Made in USA
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredients
Benzalkonium Chloride 0.13%
Purpose
First Aid Antiseptic
Uses
- First Aid to help reduce the risk of infection in minor cuts, scrapes and burns
RECENT MAJOR CHANGES SECTION
Updaed Indications & USage section to be in line with the OTC Monograph
Warnings
For external use only.
OTC - DO NOT USE SECTION
Do not use in the eyes. If this happens, rinse thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or redness develop and persists for more than 72 hours
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
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. Allow hands to dry without wiping.
INACTIVE INGREDIENT SECTION
Inactive ingredients purified water, alcohol
Made in USA
PRINCIPAL DISPLAY PANEL – packet label
Henry Schein REF112-6735
NDC 0404-6735-01
BZK TOWELETTE
Contains Benzalkonium Chloride
For External Use Only • Non-Sterile
Not Made with Natural Rubber Latex
1 single-use, premoistened towelette
Distributed by (in US only)
HENRY SCHEIN, Inc. 135 Duryea Road
Melville, NY 11747 USA
Made in China
Rev.2024/04
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0404-6735-01 | 2023-07-13 | C162847 | 48780-1 | 9d75b9d0-67bd-f424-e053-dadaa90a57ce | ANTISEPTIC – Benzalkonium chloride liquid Henry Schein |
| 0404-6735-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-67bd-f424-e053-dadaa90a57ce | ANTISEPTIC – Benzalkonium chloride liquid Henry Schein |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0404-6735-01 | BZK | 2.5 g in 1 PACKET | LIQUID | 2.5 | 5 | |
| 0404-6735-01 | BZK | 100 in 1 BOX | LIQUID | 100 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| benzalkonium chloride | ACTIVE INGREDIENT | F5UM2KM3W7 | 1 | |
| benzalkonium | ACTIVE MOIETY | 7N6JUD5X6Y | 1 | |
| alcohol | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- BZK
- benzalkonium chloride
- WATER
- BENZALKONIUM
- SODIUM BICARBONATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0404-6735 | 0404-6735-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| SODIUM BICARBONATE | 8MDF5V39QO | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| BZK | BENZALKONIUM CHLORIDE | Henry Schein Inc. | ff877b63-fa58-4770-a882-694eda33203b | 2024-04-02 | Warnings | 0404-6735-01 0404-6735 00404673501 1522e337-1394-24fa-e063-6394a90ae000 ff877b63-fa58-4770-a882-694eda33203b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.