Label: CV MEDICATED- triclosan soap
-
Contains inactivated NDC Code(s)
NDC Code(s): 0519-6262-03, 0519-6262-13, 0519-6262-41, 0519-6262-87, view more0519-6262-92, 0519-6262-94 - Packager: STERIS Corporation
- Category: HUMAN OTC DRUG LABEL
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 Label Information
Updated May 29, 2015
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
-
Warnings
For external use only
Discontinue use if irritation and redness develop. If irritation persists for more than 3 days, consult a physician.
- Directions
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
-
INGREDIENTS AND APPEARANCE
CV MEDICATED
triclosan soapProduct 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)