Septisol NPD with Triclosan Antiseptic

Dosage form: liquid
Ingredients: Triclosan 0.25mL in 100mL
Labeler: STERIS Corporation
NDC Code: 0519-1357

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.

SEPTISOL® NPD WITH TRICLOSAN
Antiseptic Handwash

Drug Facts

Active ingredient

0.25% Triclosan

Purpose

Antiseptic Handwash

Use

decreases the level of transient microorganisms on the skin

Warnings

For external use only

Stop use and ask a doctor if irritation and redness develop and persist for more than 5 days.

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 of Septisol NPD with Triclosan on the hands. Wash hands, rinse thoroughly with water, and repeat as necessary between patient contacts.

Inactive ingredients

Water, sodium C14-C16 olefin sulfonate, sorbitol, hydroxyethylecellulose, citric acid

Questions or comments?

USA 1-800-548-4873

PRINCIPAL DISPLAY PANEL - 3.78 Liter Bottle Label

NDC 0519-1357-08

SEPTISOL® NPD WITH TRICLOSAN

Antiseptic Handwash

Net Contents: 3.78 Liters (1 Gal.)
1357-08

SEPTISOL NPD WITH TRICLOSAN   ANTISEPTIC
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0519-1357
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (Triclosan) Triclosan0.25 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
water 
sodium C14-16 olefin sulfonate 
sorbitol 
citric acid monohydrate 
Product Characteristics
ColorWHITE (Off-White) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:0519-1357-083078 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E03/25/2011
Labeler - STERIS Corporation (139424188)
Establishment
NameAddressID/FEIOperations
STERIS Corporation139424188MANUFACTURE

Revised: 03/2011
 
STERIS Corporation

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.

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