TRISEPTIN  WATER AIDED- alcohol lotion 
DFB Technology 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

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:

Stop use and ask doctor if:

Keep out of reach of children. 

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

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 1-800-323-9088 (M-F 8 a.m.-5 p.m. CST).

Distributed by Becton Dickinson, El Paso, TX 79912
Manufactured for DFB Technology, Ltd., Fort Worth, TX 76107
by DPT Laboratories, Ltd., San Antonio, TX 78215


32 fl oz (1 qt)

(946 ml)
140896-0417

PRINCIPAL DISPLAY PANEL

NDC 70472-102-32

Triseptin ®
Ethyl alcohol 70% v/v
WATER-AIDED
Surgical Hand Scrub


Alcohol with Persistence™

Directions

Warnings
Flammable, keep away from fire or flame.
For external use only.
Do not use:

Stop use and ask doctor if:

Read Drug Facts Before Use.

32 fl oz (1 qt)

(946 ml)
140895-0417

BD

REORDER NO. 0064-1030-32

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

front

back

TRISEPTIN   WATER AIDED
alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70472-102
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:70472-102-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/25/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/25/2017
Labeler - DFB Technology Ltd (965516164)
Establishment
NameAddressID/FEIBusiness Operations
DPT Laboratories, Ltd.832224526manufacture(70472-102)

Revised: 9/2017
Document Id: 5902cc80-0f0c-95b8-e053-2991aa0a4862
Set id: cf2032eb-c9bd-4977-8707-f17e1e84fd91
Version: 1
Effective Time: 20170912
 
DFB Technology Ltd