TRISEPTIN- 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 Hand and Body Antiseptic

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

Surgical Hand Scrub

Patient Preoperative Skin Preparation

Warnings

Flammable, keep away from fire or flame.
For external use only.

Do not  Use:

Stop use and ask a doctor if:

Keep out of reach of chipdren.

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

Directions

Surgical Hand Scrub

Patient Preoperative Skin Preparation

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
4 fl oz (118 mL)
140840-1116

PRINCIPAL DISPLAY PANEL

NDC 70472-101-04
Triseptin®
Ethyl alcohol 70% v/v
Hand & Body Antiseptic

Surgical Hand Scrub

Patient Preoperative Skin Preparation

4 fl oz
(118 ml)
140839-1116

BD
REORDER NO. 0064-1050-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Label 4 oz

Back Label 4 oz Panel 1 of 3

Back Label 4 oz Panel 2 of 3

Back Label 4 oz Panel 3 of 3

TRISEPTIN 
alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70472-101
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:70472-101-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/15/2017
Labeler - DFB Technology Ltd (965516164)
Establishment
NameAddressID/FEIBusiness Operations
DPT Laboratories832224526manufacture(70472-101)

Revised: 12/2017
Document Id: 619a3982-a37f-7c26-e053-2991aa0a57ec
Set id: 9e576925-3519-4d07-b12e-5e3fe5460b96
Version: 1
Effective Time: 20171230
 
DFB Technology Ltd