CV MEDICATED- triclosan soap

CV Medicated by

Drug Labeling and Warnings

CV Medicated by is a Otc medication manufactured, distributed, or labeled by STERIS Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

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

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

STERIS®

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

6262-86L(F)(515)

61080

INGREDIENTS AND APPEARANCE

CV MEDICATED 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0519-6262
Route of Administration	TOPICAL

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 MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
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)