SOFT CARE FOAMING INSTANT HAND SANITIZER- benzethonium chloride liquid

Soft Care Foaming Instant Hand Sanitizer by

Drug Labeling and Warnings

Soft Care Foaming Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Diversey, Inc., Kutol Products Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzethonium Chloride 0.2%

PURPOSE

Purpose

Antiseptic handwash

INDICATIONS & USAGE

Uses

For handwashing to decrease bacteria on the skin.

WARNINGS

Warnings

Combustible liquid. Keep away from heat, sparks, or flame.

For external use only.

When using this product

Do not use in the eyes. If accidental eye contact occurs, rinse with water.

If eye irritation persists, get medical attention.

Stop use and ask a doctor if irritation and redness develop.

If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

Directions

To decrease bacteria on skin, apply small amount to palm.

Briskly rub, covering hands with product until dry.

REFERENCES

Other information

EMMERGENCY PHONE: 1-800-851-7145

See MSDS #MS0300807

See container for Lot Code and Expiry Date

For Commercial and Industrial Use Only

INACTIVE INGREDIENT

Inactive ingredients

Water, Alcohol Denat., Cocamidopropyl Betaine, Propylene Glycol, Phenoxyethanol, PEG-7 Glyceryl Cocoate, Tetrasodium EDTA, Aloe Bardadensis Leaf, Tocopheryl Acetate, Fragrance

QUESTIONS

Questions or comments?

1-800-558-2332 Monday through Friday 7:30 AM to 5:00 PM Central Standard Time

www.diversey.com

PRINCIPAL DISPLAY PANEL

Diversey

NDC: 64536-1268-1

Soft Care

Foaming Instant Hand Sanitizer

Net Contents

1 L / 1.06 U.S. Qt

5510245

INGREDIENTS AND APPEARANCE

SOFT CARE FOAMING INSTANT HAND SANITIZER 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64536-1268
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE SODIUM (UNII: MP1J8420LU)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64536-1268-1	1000 mL in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/11/2010

Labeler - Diversey, Inc. (018240817)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products Company, Inc.		004236139	manufacture