Waxman Kleen Freak Hand Sanitizer

Manufacturer
Natural Essentials, Inc.
Effective date
2020-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:14

Label at a glance#

ProductWaxman Kleen Freak Hand Sanitizer
Active ingredientAlcohol
Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame

For external use only

When using this product

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.

Other information

OTHER SAFETY INFORMATION

May discolor certain fabrics. Store under 105 F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/Vinyl Isodecanoate Crosspolymer, Aloe Barbadensis Leaf, PEG-6, PEG-12 Dimethicone, Water

May contain fragrance

Principal Display Panel – 1 Gallon Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills
99.9% of
Germs

waxman

kleen
freak™
hand sanitizer

Contains 70% alcohol
to kill common germs

1 Gallon

Principal Display Panel – 1 Gallon Bottle Label
Principal Display Panel – 1 Gallon Bottle Label

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66902-75066902-750-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
23fa1493-efa6-6366-e063-6394a90aa590603ee9c0-29cd-4fef-a5b3-d2b5d46bbd002024-10-08WarningsExact identifier
spl set id: 603ee9c0-29cd-4fef-a5b3-d2b5d46bbd00

Reported adverse events (FAERS/openFDA)#

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