CV MEDICATED- triclosan soap 
STERIS Corporation

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.

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CV® Medicated Lotion Soap

Drug Facts

Active ingredient

0.5% Triclosan

Purpose

Antiseptic

Use

Healthcare Personnel Handwash to decrease transient bacteria on the skin before contact with patients under medical care or treatment.

Warnings

For external use only

Discontinue use if irritation and redness develop. If irritation persists for more than 3 days, consult a physician.

When using this product do not get it in the eyes; this product causes eye irritation upon direct contact. In case of eye exposure, rinse thoroughly with water. If eye irritation persists, contact a physician.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Warning

This product contains a chemical known to the State of California to cause cancer.

Directions

Wet skin and spread a small amount on the hands. Wash hands, rinse thoroughly with water, and repeat as necessary between patient contacts.

Inactive ingredients

Water, alkali salts of fatty acids, sorbitol, disodium cocoamphodiacetate, cocoamide DEA, glycerin, acrylates/PEG-10 maleate/styrene copolymer, hydrolyzed collagen, tetrasodium EDTA, sodium chloride, iodopropynyl butylcarbamate, fragrance

Questions or comments?

800-548-4873 www.steris.com

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

CV® Medicated

Lotion
Soap

NDC 0519-6262-41

Hand Soap

Moisturizing

Antimicrobial

15
seconds
Fast-acting

REORDER #
6262-87

For Hospital and Professional Use Only.

1 Liter SDS (33.8 fl oz) (1.05 qt)

STERIS®

STERIS Corporation ■7501 Page Avenue ■ St. Louis, MO 63133 ■ USA

6262-86K(F)(814)

61080

Principal Display Panel - 1 Liter Bottle Label
CV MEDICATED 
triclosan soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0519-6262
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.5 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
GLYCERIN (UNII: PDC6A3C0OX)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)  
GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
Product Characteristics
Color WHITE (Off-white) Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0519-6262-94 72 in 1 CASE
1 NDC:0519-6262-03 118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2 NDC:0519-6262-92 18 in 1 CASE
2 NDC:0519-6262-13 444 mL in 1 BOTTLE; Type 0: Not a Combination Product
3 NDC:0519-6262-87 12 in 1 CASE
3 NDC:0519-6262-41 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/27/2003
Labeler - STERIS Corporation (139424188)
Establishment
Name Address ID/FEI Business Operations
STERIS Corporation 139424188 MANUFACTURE(0519-6262)

Revised: 10/2014
Document Id: d3d10a9f-68d6-42c9-a8fd-789c337bbde4
Set id: 2ab4b8aa-4878-4668-83bf-3e9ccb11341d
Version: 3
Effective Time: 20141024
 
STERIS Corporation