BACTI-FOAM- triclosan solution

Bacti-Foam by

Drug Labeling and Warnings

Bacti-Foam 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

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 INGREDIENT

​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

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

INGREDIENTS AND APPEARANCE

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)