TRISEPTIN  WATER AIDED- alcohol lotion 
HEALTHPOINT, LTD

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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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

65dd8689-figure-01
65dd8689-figure-02
TRISEPTIN   WATER AIDED
alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0064-1030
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCAMINE OXIDE (UNII: QWA2IZI6FI)  
GLYCERYL LAURATE (UNII: Y98611C087)  
HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
PYRITHIONE ZINC (UNII: R953O2RHZ5)  
Product Characteristics
Colorwhite (white to off-white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0064-1030-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/200008/25/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/200008/25/2017
Labeler - HEALTHPOINT, LTD (965634504)
Establishment
NameAddressID/FEIBusiness Operations
DPT LABORATORIES, LTD832224526manufacture(0064-1030)

Revised: 8/2017
 
HEALTHPOINT, LTD