X3 Hand Sanitizer (Spray)

Manufacturer
X3 Labs Inc. | Canadian Custom Packaging Company
Effective date
2009-08-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:22:34

Label at a glance#

ProductX3 Clean
Active ingredientBenzalkonium Chloride
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose Antimicrobial

INDICATIONS & USAGE SECTION

Use To decrease bacteria on the skin that could cause disease.

WARNINGS SECTION

Warnings For external use only. Do not freeze.

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

OTC - STOP USE SECTION

Stop use and ask doctor if skin irritation 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 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.

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 SprayPSN2
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD2
1039012benzalkonium chloride 0.13 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
26550-001-102020-01-31C16284748780-19d75b9cf-d99a-f424-e053-dadaa90a57ceX3 Hand Sanitizer (Spray)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
26550-001-10X3 Clean8 mL in 1 BOTTLESPRAY82

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
26550-001X3 CLEAN (HAND SANITIZER SPRAY) SPRAY [X3 LABS INC.]2Current NDC, Legacy NDC, 1 package rows20090901_cfd183f7-e2f8-44a4-a4d0-fc8823385056.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W72
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y2
Cocamidopropyl BetaineINACTIVE INGREDIENT5OCF3O11KX2
GlycerinINACTIVE INGREDIENTPDC6A3C0OX2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
26550-00126550-001-10

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GlycerinGLYCERINPDC6A3C0OXAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
X3 CleanBENZALKONIUM CHLORIDEX3 Labs Inc.a8eedcfd-3b97-497a-9a34-d59b0dd784392025-09-03WarningsExact identifier
ndc (product): 26550-001
e3c9449c-64c1-4964-a1ec-2636c0aeb29ccfd183f7-e2f8-44a4-a4d0-fc88233850562009-08-24WarningsExact identifier
spl id: e3c9449c-64c1-4964-a1ec-2636c0aeb29c
spl set id: cfd183f7-e2f8-44a4-a4d0-fc8823385056

Reported adverse events (FAERS/openFDA)#

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