FDA.reportPublic FDA data

X3 Hand Sanitizer (Spray)

Manufacturer
X3 Labs Inc.
Effective date
2025-09-03
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:12:27

Label at a glance#

ProductX3 Clean
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For external use only. Do not freeze. Do not use in or near eyes. In case of contact with eyes, flush thoroughly with water.




Stop use and ask doctor

OTC - STOP USE SECTION

if skin irritation develops.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions Apply a small amount to palms and rub hands thoroughly until completely dry.

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin, Cocamidopropyl Bentaine.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0.27 oz Hand Sanitizer Spray
0.27 oz Hand Sanitizer Spray

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN6
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD6
1039012benzalkonium chloride 0.13 % Topical SpraySY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
26550-002-10X3 Clean8 mL in 1 BOTTLESPRAY86

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
26550-00226550-002-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
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
X3 CleanBENZALKONIUM CHLORIDEX3 Labs Inc.40cc6501-3cee-24cc-e054-00144ff88e882025-09-03WarningsExact identifier
ndc (package): 26550-002-10
ndc (product): 26550-002
ndc11 (package): 26550000210
spl id: 3de94ba3-488b-7e1a-e063-6294a90a1e03
spl set id: 40cc6501-3cee-24cc-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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