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Soft Care Foam Antibacterial Hand Soap

Dosage form: liquid
Ingredients: Triclosan 0.5mL in 100mL
Labeler: Johnson Diversey, Inc.
NDC Code: 64536-3851

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredient                                                            Purpose

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


For handwashing to decrease bacteria on the skin.


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.


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


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

Soft Care

Foam Antibacterial Hand Soap

NDC 064536-3851-1


Made in U.S.A.

1 L  1.06 U.S. Qt.

triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64536-3851
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (Triclosan) Triclosan0.5 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Ammonium Lauryl Sulfate 
Aloe Vera Leaf 
Citric Acid Monohydrate 
Cocamide Diethanolamine 
DMDM Hydantoin 
Sodium Laureth Sulfate 
FD&C Yellow No. 5 
#Item CodePackage Description
1NDC:64536-3851-11000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33304/30/2010
Labeler - Johnson Diversey, Inc. (018240817)
Kutol Products Co Inc004236139manufacture

Revised: 06/2010
Johnson Diversey, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.