BACTI-FOAM- triclosan solution 
Ecolab Inc.

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.

----------

Drug Facts

Active Ingredient

Triclosan, 0.3%

Purpose

Healthcare personnel handwash

Uses

  • healthcare personnel handwash

Warnings

  • For external use only

When using this product

  • discontinue use if irritation and redness develop

Stop use and ask 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 apply a small amount on hands and forearms
  • scrub well, rinse thoroughly and dry

Other information

  • for emergency medical information in USA and Canada, call 1.800.328.0026
  • for emergency medical information worldwide, cal 1.651.222.5352 (in the USA)

​Inactive ingredients water, potassium cocoate, SD alcohol 40-B, glycerin, potassium stearate, tetrasodium EDTA, cocamidopropyl PG-dimonium chloride phosphate, cocamine oxide, fragrance, methylparaben, tocopheryl acetate, citric acid, potassium hydroxide, isopropyl alcohol, propylparaben, aloe barbadensis leaf juice, FDC blue 1, FDC yellow 5

Questions? call​ 1.866.781.8787

Principal Display Panel and Representative Label

ECOLAB®

NDC 47593-169-56
DIN 02237409

BACTI-FOAM®

Antimicrobial Foam Hand Soap

Healthcare Peronnel Handwash

Active Ingredient:  0.3% Triclosan

Nets Contents:

1200 mL (40.6 fl oz)

6082565

747795/8502/1012

representative label

BACTI-FOAM 
triclosan solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-169
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM STEARATE (UNII: 17V812XK50)  
EDETATE SODIUM (UNII: MP1J8420LU)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
COCAMINE OXIDE (UNII: QWA2IZI6FI)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47593-169-38500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/08/201212/19/2018
2NDC:47593-169-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/13/201312/19/2018
3NDC:47593-169-561200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/30/200912/19/2018
4NDC:47593-169-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/30/200912/19/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/11/199712/19/2018
Labeler - Ecolab Inc. (006154611)

Revised: 1/2021
 
Ecolab Inc.