BACTI-STAT AE- triclosan solution

Bacti-Stat AE by

Drug Labeling and Warnings

Bacti-Stat AE 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 or redness persists 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, cocamidopropyl PG-dimonium chloride phosphate, potassium stearate, tetrasodium EDTA, hydroxyethylcellulose, fragrance, cocamine oxide, methylparaben, tocopheryl acetate, citric acid, isopropyl alcohol, propylparaben, aloe barbadensis leaf juice, FD&C blue 1, FD&C yellow 5

QUESTIONS

​Questions? ​call 1.866.781.8787

Principal Display Panel and Representative Label

ECOLAB

NDC: 47593-170-31

BACTI-STAT AE®

Antimicrobial Hand Soap

Formulated with Aloe Vera & Vitamin E

to promote skin health

Healthcare personnel handwash

Active Ingredient: 0.3% Triclosan

6060116

Net Contents: 540 mL (18 fl oz)

Ecolab · 370 Wabasha Street N ·
St Paul MN 55102-1390 USA
© 2012 Ecolab USA Inc · All rights reserved
Made in United States
www.ecolab.com · 704451/8500/1012
SDS-IN-1633

INGREDIENTS AND APPEARANCE

BACTI-STAT AE 
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-170
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)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
POTASSIUM STEARATE (UNII: 17V812XK50)
EDETATE SODIUM (UNII: MP1J8420LU)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-170-31	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/21/2012
2	NDC: 47593-170-32	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/21/2012
3	NDC: 47593-170-26	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/21/2012
4	NDC: 47593-170-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/12/2009	04/27/2016
5	NDC: 47593-170-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/22/2013	04/27/2016
6	NDC: 47593-170-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/22/2013	04/27/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/14/1997

Labeler - Ecolab Inc. (006154611)