FDA.reportPublic FDA data

WOW QUICK KILL BAC

Manufacturer
EZ Finishes Inc | Enzyme Solutions, Inc.
Effective date
2020-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:23:15

Label at a glance#

ProductWOW QUICK KILL BAC
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply to hands and rub lightly until dry without wiping or rinsing.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin

  • If hands are visibly soiled, use regular soap and water
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For External Use only

OTC - WHEN USING SECTION

When using this product do not get in eyes.

If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops.

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:

DOSAGE & ADMINISTRATION SECTION

Apply to hands and rub lightly until dry without wiping or rinsing.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Dihydroxy-propyl PEG-5 Limoleammonia Chloride, Glycereth-2 Cocoate, Behentrimonium Chloride, Dihydroxyethyl Cocamine Oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WOW!

EZ FINISHES

WOW! QUICK KILL BAC

Non-Alchol Foam Hand Sanitier

Tough on Germs

Gentle on Skin

NDC# 79354-001-01

Safely Kills Germs on Hands Immediately

Anti-Baterial

Extended Protection

No Alcohol and no harsh chemical leaves

skin soft after use

MADE IN THE U.S.A.

1 Gallon (3.78 L)

container labelcontainer label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79354-00179354-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f1ecb12e-731a-74b1-e053-2995a90ace9da93fcecb-d0cc-56ed-e053-2995a90a82692023-01-10WarningsExact identifier
spl set id: a93fcecb-d0cc-56ed-e053-2995a90a8269

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.