FDA.reportPublic FDA data

Kleen Freak Disinfecting Wipes

Manufacturer
Zhejiang Ruolin Hygienic Products Co., Ltd.
Effective date
2020-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:56

Label at a glance#

ProductKleen Freak Disinfecting Wipes
Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL
Label structure6 sections

Dosage and administration

Wipe surface with product and allow to dry Discard wipes in trash receptacle after use. Do not flush. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Alcohol 4%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warning

WARNINGS SECTION

  • For external use only.
  • When using this product, Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
  • Stop use and ask a doctor, if irritaion and rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Contrl Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe surface with product and allow to dry
  • Discard wipes in trash receptacle after use. Do not flush.
  • Children under 6 years of age should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Ehtylhexylglycerin, Didecyldimethylemmonium CHLORIDE, Phenoxyethanol, Alcohol, Propylene Glycol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label imagelabel image

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130028905305013GTIN-13: 0028905305013
EAN-13: 0028905305013
GTIN-12: 028905305013
UPC-A: 028905305013
GTIN storage (14 digits): 00028905305013		Kleen Freak Disinfecting Wipes bzk alcohol 70 pcs.jpg

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78823-03778823-037-01

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
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALCOHOL3K9958V90MACTIB
water059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT

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
1badb849-675b-1246-e063-6394a90a5603fa538bab-4c06-4651-8e7e-9ed867e580502024-06-24WarningsExact identifier
spl set id: fa538bab-4c06-4651-8e7e-9ed867e58050

Reported adverse events (FAERS/openFDA)#

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