SOFT CARE ANTISEPTIC SKIN CLEANSER II- triclosan liquid
Diversey, Inc.

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Drug Facts

Active ingredient

Triclosan 0.55%

Purpose

Antiseptic handwash

Uses

For hand washing to decrease bacteria on skin.

Warnings

For external use only. Do not ingest.

When using this product

Do not use in the eyes.

In case of contact, immediately flush with water.

Stop use and ask a doctor if

irritation and redness develops.

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.

Directions

To decrease bacteria on skin.

Use 5 mL (sufficient amount to cover hands with product) and lather in hands with water for at least 30 seconds.

Rinse well with potable water.

Avoid contamination of food during use and storage.

Inactive ingredients

Water, Ammonium lauryl sulfate, Sodium laureth sulfate, Sodium chloride, Cocamidopropyl betaine, Disodium cocamido MIPA-sulfosuccinate, BHT, Styrene/acrylates copolymer, Glycerin, DMDM hydantoin, Tetrasodium EDTA, Citric acid, Fragrance

Questions or comments?

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

Central Standard Time

www.diversey.com

Other information

EMERGENCY PHONE: 1-800-851-7145

See SDS # MS0301401

FOR COMMERCIAL AND INDUSTRIAL USE ONLY

See Carton for Lot Code and Expiry Date.

Sealed Air

Diversey Care

Diversey

Soft Care

Antiseptic Skin

Cleanser II

NDC 64536-7090-1

Triclosan lotion

DIN 02417324

Product of U.S.A.

Net Contents

1 L/1.06 U.S. Qt.

5982875

container label

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SOFT CARE ANTISEPTIC SKIN CLEANSER II
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:64536-7090
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.55 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
GLYCERIN (UNII: PDC6A3C0OX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:64536-7090-4	600 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/09/2014	02/14/2018
2	NDC:64536-7090-1	1000 mL in 1 BAG; Type 0: Not a Combination Product	06/09/2014	02/14/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	06/09/2014	02/14/2018

Labeler - Diversey, Inc. (018240817)

Name	Address	ID/FEI	Business Operations
Establishment
Kutol Products Company Inc		004236139	manufacture(64536-7090)

Revised: 11/2023

Document Id: 0a34706b-1e25-3e15-e063-6394a90a0327

Set id: 2b972659-629e-4805-9489-5a92d4a3e1cd

Version: 2

Effective Time: 20231115

Diversey, Inc.