Crazy Cleanz Foaming Hand Sanitizer - Eucalyptus

Manufacturer
WeCool Toys, Inc. | Landy International
Effective date
2022-01-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:17:56

Label at a glance#

ProductCrazy Cleanz Foaming Hand Sanitizer - Eucalyptus
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Storage and handling

Other Information *Store between 15-30C (56-86F) *Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT(S) Purpose

Benzalkonium Chloride 0.10%..................Antiseptic

OTC - PURPOSE SECTION

Use(s): Helps eliminate bacteria on hands.

WARNINGS SECTION

WARNINGS: For external use only

INDICATIONS & USAGE SECTION

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 occures. 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.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

* 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.

STORAGE AND HANDLING SECTION

Other Information

*Store between 15-30C (56-86F)

*Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Deionized water
Glycerin
Didecyldimonium chloride
FD&C Blue 1
FD&C Yellow 5
Fragrance - Eucalyptus
Limonene
Linalool

PEG-40 hydrogenated castor oil

Polyaminopropyl biguanide

RECENT MAJOR CHANGES SECTION

Changed title of sections.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 77006-010

RNLabelRNLabel

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77006-01077006-010-01, 77006-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
2d57f1f3-d9ab-c47c-e063-6294a90a309aa6a7683a-cefc-cefd-e053-2995a90a9cb52025-02-04WarningsExact identifier
spl set id: a6a7683a-cefc-cefd-e053-2995a90a9cb5

Reported adverse events (FAERS/openFDA)#

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