Drug Facts

Active ingredient Purpose

Triclosan 0.5%...............................................................Antiseptic Handwash

Uses

For handwashing to decrease bacteria on the skin.

Warnings

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 conditions 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

Use as part of a daily cleansing routine.

To decrease bacteria on the skin, apply sufficient amount to cover hands with product.

Wash Hands.

Other information

EMERGENCY PHONE: 1-800-851-7145

See MSDS MS0127198

See container for Lot Code and Expiry Date

FOR COMMERCIAL AND INDUSTRIAL USE ONLY

Inactive ingredients

Water Ammonium Lauryl Sulfate, Aloe Barbensis Leaf, Citric Acid, Cocamide DEA, Disodium Cocamide MIPA-Sulfosuccinate, DMDM Hydantoin, Glycerin, Polyquaternium-7, Polyquaternium-10, Sodium Laureth Sulfate, Tetrasodium EDTA, Tocopheryl Acetate, Fragrance, Red 33, Yellow 5.

Questions or comments?

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

www.johnsondiversey.com

Purpose

Antiseptic Handwash

Soft Care

Foam Antibacterial Hand Soap

NDC 064536-3851-1

Made in U.S.A.

1 L 1.06 U.S. Qt.

container label

SOFT CARE FOAM ANTIBACTERIAL HAND
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:64536-3851
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)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:64536-3851-1	1000 mL in 1 BAG; Type 0: Not a Combination Product	04/30/2010	10/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	04/30/2010	10/01/2016

Labeler - Johnson Diversey, Inc. (018240817)

Name	Address	ID/FEI	Business Operations
Establishment
Kutol Products Co Inc		004236139	manufacture(64536-3851)

Revised: 11/2023

Document Id: 0a36319e-9ac5-1190-e063-6294a90aef9a

Set id: 9e01f5af-81ca-4dfe-8f27-d803bc7c29d9

Version: 2

Effective Time: 20231115

Johnson Diversey, Inc.