Kleen Freak hand sanitizer

Manufacturer: Guangzhou Minghui Cosmetics Co., Ltd.
Effective date: 2020-07-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:21:48

Label at a glance#

ProductKleen Freak hand sanitizer

Active ingredientALCOHOL

Label structure6 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% (V/V)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce germs on the skin that an potntially cause disease. Use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only.

Flammable,

Keep away from fire or flame

When using this product do not use in or near the eyes

In case of contact, rinse eyes thoroughly with water.

Discontinue use and ask a doctor if

irritation or rash appears and lasts.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product.
Rub hands together for no less than 15 seconds
Allow to dry without wiping or rub hands together briskly until dry
Store in a cool dry place below 104℉

Inactive ingredients

INACTIVE INGREDIENT SECTION

Capom, Propylene Glycol, Allantoin, EDTA-2Na, Trimethylglycine, Methyl ESter, Sodium Hydroxide, DMDM Hydantoin, PEG-40 Hydrogenated Castor Oil

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1047755	ethanol 75 % Topical Solution	PSN	1
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	1
1047755	ethanol 75 % Topical Solution	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d1c9d1af-bddd-448d-86f7-69052b7d5b47	Product name	1	20220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74447-106-01	2022-01-28	C162847	48780-1	d6a99b39-c516-a426-e053-dadaa90af4c2	91b6c62d-d42d-4b0c-a138-ae64d356b1e9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74447-106-01	Kleen Freak hand sanitizer	500 mL in 1 BOTTLE	LIQUID	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74447-106	KLEEN FREAK HAND SANITIZER (ALCOHOL) LIQUID [GUANGZHOU MINGHUI COSMETICS CO., LTD.]	1	Legacy NDC, 1 package rows	20200718_91b6c62d-d42d-4b0c-a138-ae64d356b1e9.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Kleen Freak hand sanitizer
Alcohol
PROPYLENE GLYCOL
ALLANTOIN
BETAINE
METHYL 2-FUROATE
SODIUM HYDROXIDE
DMDM HYDANTOIN
POLYOXYL 40 HYDROGENATED CASTOR OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74447-106	74447-106-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALLANTOIN	344S277G0Z	IACT
BETAINE	3SCV180C9W	IACT
METHYL 2-FUROATE	O9A8D29YDE	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
8b9cc436-f04f-4f0a-9155-77f22f62de34			91b6c62d-d42d-4b0c-a138-ae64d356b1e9	2020-07-18	Warnings	Exact identifier spl id: 8b9cc436-f04f-4f0a-9155-77f22f62de34 spl set id: 91b6c62d-d42d-4b0c-a138-ae64d356b1e9

Reported adverse events (FAERS/openFDA)#

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