FDA.reportPublic FDA data

Waxman Kleen Freak Disinfecting Wipes

Manufacturer
WAXMAN CONSUMER PRODUCTS GROUP INC. | Zhejiang Ruolin Hygienic Products Co., Ltd. | Guangzhou Daieme Cosmetic Co., Ltd.
Effective date
2020-10-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:10:02

Label at a glance#

ProductWaxman Kleen Freak Disinfecting Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Wet hands thoroughly 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 Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonmium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

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

In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly 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, Ethylhexylglycerin, Phenoxyethanol, Didecydimethylammonium Chloride, Propylene Glycol, Fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills

99.9%

of Germs*

waxman

kleen

freak

disinfecting wipes

one-step hand-cleaning and disinfecting

70 sheets 5.51 in x 7.87 in (14.0 cm x 20.0 cm) 14.8 oz (420 g)

container labelcontainer label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80765-003-702022-07-29C16284748780-1e4f33bdf-a6c3-d8a0-e053-dadaa90a6e4eb283f37c-a974-4066-e053-2a95a90a680a

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80765-00380765-003-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
WATER059QF0KO0RIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
e4f4e282-345f-cb1c-e053-2a95a90a3ae3b283f37c-a974-4066-e053-2a95a90a680a2022-07-29WarningsExact identifier
spl set id: b283f37c-a974-4066-e053-2a95a90a680a

Reported adverse events (FAERS/openFDA)#

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