BACTI-STAT- triclosan solution

Bacti-Stat by

Drug Labeling and Warnings

Bacti-Stat by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Triclosan, 0.3%

Purpose

Healthcare personnel handwash

Uses

healthcare personnel handwash

Warnings

• For external use only
  

Do not use

• in eyes
  

When using this product

• discontinue use if irritation and redness develop

Stop use and ask a doctor if

• skin irritation and redness persist for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet skin and spread a small amount on hands and forearms
• scrub well, rinse thoroughly and dry
  

Other information

• For additional information, see Material Safety Data Sheet (MSDS)
• For emergency medical information in USA and Canada, call 1-800-328-0026
• For emergency medical information worldwide, call 1-651-222-5352 (in the USA)
  

INACTIVE INGREDIENT

Inactive ingredients water, potassium cocoate, SD alcohol 40-B, glycerin, potassium stearate, cocamidopropyl PG-dimonium chloride phosphate, tetrasodium EDTA, hydroxyethylcellulose, cocamine oxide, fragrance, methylparaben, tocopheryl acetate, citric acid, isopropyl alcohol, propylparaben, aloe barbadensis leaf juice, D&C red 33

QUESTIONS

Questions? call 1 866 781 8787

Principal Display Panel and Representative Label

ECOLAB®

NDC: 47593-178-26

BACTI-STAT®

Antimicrobial Hand Soap

Healthcare Personnel Handwash

Active Ingredient: 0.3% Triclosan

6023426

Net Contents: 1000 mL (33.8 fl oz)

Ecolab - 370 Wabasha St N - St Paul MN

55102-1390 USA

©2012 Ecolab USA Inc. - All rights reserved

Made in United States

www.ecolab.com - 704446/8500/1012

SD-IN-1633

INGREDIENTS AND APPEARANCE

BACTI-STAT 
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-178
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	3.06 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM STEARATE (UNII: 17V812XK50)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
EDETATE SODIUM (UNII: MP1J8420LU)
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%) (UNII: 7Q6P4JN1QT)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-178-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/1997
2	NDC: 47593-178-33	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/1997
3	NDC: 47593-178-31	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/1997
4	NDC: 47593-178-32	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/23/1997
5	NDC: 47593-178-26	1000 mL in 1 BAG; Type 0: Not a Combination Product	01/23/1997

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/23/1997

Labeler - Ecolab Inc. (006154611)