FDA.reportPublic FDA data

ZUDZ HAND SANITIZER

Manufacturer
Katan Tech / Quality Blending | Portofino & Associates, LLC.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:36

Label at a glance#

ProductZUDZ HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Benzalkonium Chloride 0.13%........................ Antimicrobial

OTC - PURPOSE SECTION

Uses

• For hand sanitizing to decrease bacteria on the skin • Recommended for repeated use

INDICATIONS & USAGE SECTION

Uses

• For hand sanitizing to decrease bacteria on the skin • Recommended for repeated use

WARNINGS AND PRECAUTIONS SECTION

Warnings
For external use only

WARNINGS SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or it conditions 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.

DOSAGE & ADMINISTRATION SECTION

Apply small quantity to hands. Rub thoroughly to cover hands and fingers.

INSTRUCTIONS FOR USE SECTION

Directions

• Pump a small amount into palm of hand
• Rub thoroughly over all surfaces of both hands • Rub hand together briskly until dry

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Polysilsesquioxane Steardimonium Chloride

Contact:

OTC - QUESTIONS SECTION

Vanalay
6812 Hemlock Lane

Maple Grove,

MN 55369

Vanalay.com

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Active ingredients Purpose

Benzalkonium Chloride 0.13%........................ Antimicrobial

ZUDZ LabelZUDZ Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71315-900-192022-08-31C16284748780-1e4f33bdf-b0d8-d8a0-e053-dadaa90a6e4eZUDZ HAND SANITIZER
71315-900-382022-08-31C16284748780-1e4f33bdf-b0d8-d8a0-e053-dadaa90a6e4eZUDZ HAND SANITIZER
71315-900-992022-08-31C16284748780-1e4f33bdf-b0d8-d8a0-e053-dadaa90a6e4eZUDZ HAND SANITIZER
71315-900-192022-07-29C16284748780-1e4f33bdf-b0d8-d8a0-e053-dadaa90a6e4eZUDZ HAND SANITIZER
71315-900-382022-07-29C16284748780-1e4f33bdf-b0d8-d8a0-e053-dadaa90a6e4eZUDZ HAND SANITIZER
71315-900-992022-07-29C16284748780-1e4f33bdf-b0d8-d8a0-e053-dadaa90a6e4eZUDZ HAND SANITIZER

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71315-90071315-900-99, 71315-900-38, 71315-900-19

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDEIQ36O85WQ4IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
e78cd11c-f801-a7ce-e053-2995a90a4c27b0b3f7c8-25ed-6ba1-e053-2995a90a55d62022-08-31WarningsExact identifier
spl set id: b0b3f7c8-25ed-6ba1-e053-2995a90a55d6

Reported adverse events (FAERS/openFDA)#

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