FDA.reportPublic FDA data

Active Ingredient

Manufacturer
KLEAN FREAK, LLC
Effective date
2026-11-02
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-11-10 04:04:41

Label at a glance#

ProductKlean Freak
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Tear open package at edges, wipe down that dirty body ... yep ... even all those nooks and crannies chuck that wipe and get on with your day.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% w/w.

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When using this productdo not use in or near eyes. If contact occurs, flush thoroughly with water.

Stop useif irritation develops. If condition remains over 72 hours, contact a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenunless under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open package at edges, wipe down that dirty body ... yep ... even all those nooks and crannies chuck that wipe and get on with your day.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Waitch Hazel extract, Cocamidopropyl Betanine, Dipropylene Glycol, Aloe Vera leaf juice, Sweet Chestnut leaf extract, Disodium Cocoamphodiacetate, Chamomile flower extract, Calendula extract, Allantoin, Sodium Benzoate, Citric Acid, Tocopherol, Phenoxyethanol, Fragrance.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.instagram.com/ThekleanfreakImage-005.jpg

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78982-00578982-005-01, 78982-005-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
WITCH HAZEL101I4J0U34IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
DIPROPYLENE GLYCOLE107L85C40IACT
ALOE VERA LEAFZY81Z83H0XIACT
CASTANEA SATIVA LEAFIV3S2HH53GIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
CHAMAEMELUM NOBILE FLOWERO2T154T6OGIACT
CALENDULA ARVENSIS LEAF3U3U118F2LIACT
ALLANTOIN344S277G0ZIACT
SODIUM BENZOATEOJ245FE5EUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
TOCOPHEROLR0ZB2556P8IACT
PHENOXYETHANOLHIE492ZZ3TIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-11-28full-release2026-06-01 01:18:35

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
Klean FreakBENZALKONIUM CHLORIDEKLEAN FREAK, LLCcef2d3d4-bd5f-4f2a-bb2d-5292b78501c12025-11-28WarningsExact identifier
ndc (package): 78982-005-01
ndc (package): 78982-005-02
ndc (product): 78982-005
ndc11 (package): 78982000502
ndc11 (package): 78982000501
spl set id: cef2d3d4-bd5f-4f2a-bb2d-5292b78501c1

Reported adverse events (FAERS/openFDA)#

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