Drug Facts NDC 64536-2222

Active ingredient

Triclosan 0.5%

Purpose

Antiseptic Handwash

Uses

For handwashing to decrease bacteria on skin.

Warnings

For external use only.

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

Discontinue use 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.

Directions FOR INSTITUTIONAL AND CANADIAN FOOD PLANT USE.

To decrease bacteria on skin, wet hands and apply a dose of FOAM SELECT soap.

Rub hands together to lather for 20 seconds, rinse with potable water and dry thoroughly.

Avoid contamination of food during use and storage.

Other information

EMERGENCY PHONE: 1-800-851-7145

See MSDS MS0300942

See Carton for Lot Code and Expiry Date

FOR COMMERCIAL AND INDUSTRIAL USE ONLY

Inactive ingredients

Water, Citric Acid, Diethanolamine, Sodium Laureth Sulfate, Sodium Cumenesulfonate, Cocamidopropyl Betaine, Sodium Hydroxide, Propylene Glycol, Triethylene Glycol, Benzyl Alcohol, Magnesium Chloride, Magnesium Nitrate, Methylchloroisothiazolinone, Methylisothiazolinone

Questions or comments?

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

www.diversey.com

Diversey

NDC 64536-222-5

Soft Care

Foam Select

Antibacterial Hand Soap

DIN 02249588

READ BACK/SIDE PANEL CAREFULLY

Net Contents

800 mL/1.69 U.S. Pt.

3042222

container label

SOFT CARE FOAM SELECT ANTIBACTERIAL HAND
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:64536-2222
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.5 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIETHANOLAMINE (UNII: AZE05TDV2V)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM CUMENESULFONATE (UNII: 5798KA13PG)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
BENZYL ALCOHOL (UNII: LKG8494WBH)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:64536-2222-5	800 mL in 1 BAG; Type 0: Not a Combination Product	03/15/2013	11/21/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	03/15/2013	11/21/2015

Labeler - Diversey, Inc. (018240817)

Name	Address	ID/FEI	Business Operations
Establishment
Technical Concepts Bentfield b.v.		489421698	manufacture(64536-2222)

Revised: 12/2023

Document Id: 0c02c592-7161-8490-e063-6294a90a2cb5

Set id: 102a7429-328d-4a6b-9c56-a92bf8bd5ef4

Version: 2

Effective Time: 20231208

Diversey, Inc.