Crazy Cleanz Hand Sanitizer Eucalyptus Scented

Manufacturer
Landy International
Effective date
2022-03-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:05:34

Label at a glance#

ProductCrazy Cleanz Hand Sanitizer Eucalyptus Scented
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

-Place enough product on hands to cover all surfaces. · Rub hands together until dry. .Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands

Warnings

WARNINGS SECTION

For external use only
Do not use
. In children less than 2 months of age. On open skin wounds
When using this product keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thouroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
These may be a sign of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except under adult supervision.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

-Place enough product on hands to cover all surfaces.
· Rub hands together until dry.
.Supervise children under 6 years of age when using this product
to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Blue 1(Cl 42090), Didecyldimonium chloride,Fragrance(Parfum),Glycerin,
PEG-40 hydrogenated castor oil, Polyaminopropyl biguanide,
Water(Aqua),Yellow 5(C119140).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-95451706-954-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
23cc9979-57a3-a031-e063-6394a90a4798af63761c-b5a8-1d52-e053-2995a90ab14e2024-10-06WarningsExact identifier
spl set id: af63761c-b5a8-1d52-e053-2995a90ab14e

Reported adverse events (FAERS/openFDA)#

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