SOFT CARE IMPACT ALCOHOL FEE INSTANT HAND SANITIZER- benzalkonium chloride solution
Diversey, Inc.

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Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

Antiseptic/Antibacterial cleanser to decrease bacteria on the skin.

For occasional use.

Warnings

For external use only.

Do not ingest

Do not use in the eyes.

When using this product

do not use in the eyes.

In case of eye contact, immediately flush with water.

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.

Do not use if you are allergic to any ingredients

Directions

Apply 0.4-1ml into hands.

Rub thoroughly into hands for at least 30 seconds.

Allow to dry.

Supervise children when using this product.

Other information

EMERGENCY PHONE: 1-800-851-7145

See SDS MS0301542

FOR COMMERCIAL USE.

See container for Lot Code and Expiry Date.

Store in a cool dry place.

Inactive ingredients

Water (Aqua), Phenoxyethanol, Propylene Glycol, Glycerin, Tetrasodium EDTA, Cocamidopropyl betaine, Lauramine oxide, Citric acid

Questions or comments?

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

www.sealedair.com

NDC 64536-8398-3

DIN 02449412

Sealed Air

Diversery Care

Diversey

Soft Care

Impact Alcohol Free

Instant Hand Sanitizer

Benzalkonium Chloride Liquid

For commercial use

(L) Exp.

Net Contents

1.3 L / 1.37 U.S. Qt.

100907875

container labelFP1

container labelBP1

SOFT CARE IMPACT ALCOHOL FEE INSTANT HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:64536-8398
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:64536-8398-3	1300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/14/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	09/14/2016	04/06/2018

Labeler - Diversey, Inc. (018240817)

Name	Address	ID/FEI	Business Operations
Establishment
Diversey Canada, Inc.		249266974	manufacture(64536-8398)

Revised: 11/2023

Document Id: 09b8bdf5-71e3-ec54-e063-6294a90a489f

Set id: 1db2d206-3667-4dbe-84d1-7cc1943fa864

Version: 2

Effective Time: 20231109

Diversey, Inc.