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.

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Drug Facts

Active Ingredient

Triclosan, 0.3%

Purpose

Healthcare personnel handwash

Uses

Warnings

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

Other information

​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 Type HUMAN OTC DRUG Item Code (Source) NDC:47593-169
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 3 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)  
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:47593-169-38 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/08/2012
2 NDC:47593-169-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/13/2013
3 NDC:47593-169-56 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/30/2009
4 NDC:47593-169-59 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/30/2009
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 07/11/1997
Labeler - Ecolab Inc. (006154611)

Revised: 10/2016
Document Id: 7288a68f-da3c-494e-ab21-37d395969857
Set id: af3a3c04-5d55-46d6-bbf5-db8dfc7b9484
Version: 5
Effective Time: 20161018
 
Ecolab Inc.