TRISEPTIN WATER AIDED

Dosage form: lotion
Ingredients: ALCOHOL .7mL in 1mL
Labeler: HEALTHPOINT, LTD
NDC Code: 0064-1030

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.

TRISEPTIN Water-Aided Surgical Hand Scrub – alcohol lotion
CareFusion

Drug Facts

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Uses

Surgical Hand Scrub: Significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care.

Warnings
  • Flammable, keep away from fire or flame.
  • For external use only.
  • Do not use
  • if you are allergic to or have a known or suspected hypersensitivity to any ingredient in this product.
  • on or near the eyes, mucous membranes, genital skin, or mouth.  If product gets into the eyes, flush immediately with water.
  • Avoid contact with broken skin.
  • Stop use and ask doctor if irritation and redness develop. If condition persists for more than 72 hours consult a physician.
  • Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Clean under nails with a nail pick.  Nails should be maintained with a 1 mm free edge.
  • Wet hands and forearms.
  • Dispense palmful (approx. 7 ml) of TRISEPTIN Scrub into the palm of one hand.
  • Twist fingertips of the opposite hand, working TRISEPTIN under the nails.
  • Transfer TRISEPTIN to the opposite hand and repeat with fingertips of the other hand.
  • Rub TRISEPTIN over the hands and up the forearms to just past the elbow, paying particular attention to the nails, cuticles and interdigital spaces for 90 seconds.
  • Rinse and repeat the procedure to just below the elbows.
  • Rinse completely.

Other information

  • Store upright at 20-25°C (68-77°F).
  • Avoid freezing and excessive heat.
  • Protect from light until use.
  • Shake well.

Inactive ingredients

Benzethonium chloride, citric acid, cocamine oxide, fragrance, glyceryl laurate, hydroxypropylcellulose, phenylethyl alcohol, phosphoric acid, polyoxyl 40 stearate, propyl gallate, propylene glycol, purified water, zinc pyrithione.

Questions?

Please call 1-800-523-0502 (M-F 8 a.m.-5 p.m. CST) or visit our web site www.triseptin.com.

Marketed by CareFusion, Leawood, KS 66211
Manufactured for Healthpoint, Ltd., Fort Worth, TX 76107
by DPT Laboratories, Ltd., San Antonio, Texas 78215

REORDER NO. 0064-1030-32 PATENT NO. 6,110,908

32 fl oz (1 qt) (946 ml)
129480-0411

PRINCIPAL DISPLAY PANEL

NDC 0064-1030-32
Triseptin®
Ethyl alcohol 70% v/v
WATER-AIDED
Surgical Hand Scrub

Alcohol with Persistence™

Directions:

  • Clean under nails with a nail pick.  Nails should be maintained with a 1 mm free edge.
  • Wet hands and forearms.
  • Dispense palmful (approx. 7 ml) of TRISEPTIN Scrub into the palm of one hand.
  • Twist fingertips of the opposite hand, working TRISEPTIN under the nails.
  • Transfer TRISEPTIN to the opposite hand and repeat with fingertips of the other hand.
  • Rub TRISEPTIN over the hands and up the forearms to just past the elbow, paying particular attention to the nails, cuticles and interdigital spaces for 90 seconds.
  • Rinse and repeat the procedure to just below the elbows.
  • Rinse completely.

Warnings:

  • Flammable, keep away from fire or flame.
  • For external use only.
  • Do not use
  • if you are allergic to or have a known or suspected hypersensitivity to any ingredient in this product.
  • or on or near the eyes, mucous membranes, genital skin, or mouth.  If product gets into the eyes, flush immediately with water.
  • Avoid contact with broken skin.
  • Stop use and ask doctor if irritation and redness develop. If condition persists for more than 72 hours consult a physician.

Read Drug Facts Before Use.

32 fl oz (1 qt) (946 ml)
129479-0411

CareFusion

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
TRISEPTIN  WATER AIDED
alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0064-1030
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE 
CITRIC ACID MONOHYDRATE 
COCAMINE OXIDE 
GLYCERYL LAURATE 
HYDROXYPROPYL CELLULOSE 
PHENYLETHYL ALCOHOL 
PHOSPHORIC ACID 
POLYOXYL 40 STEARATE 
PROPYL GALLATE 
PROPYLENE GLYCOL 
WATER 
PYRITHIONE ZINC 
Product Characteristics
ColorWHITE (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:0064-1030-32946 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2000
Labeler - HEALTHPOINT, LTD (965634504)
Establishment
NameAddressID/FEIOperations
DPT LABORATORIES, LTD832224526MANUFACTURE

Revised: 01/2012
 
HEALTHPOINT, LTD

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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