SWISHER TF- benzalkonium chloride solution

Swisher TF by

Drug Labeling and Warnings

Swisher TF by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses

• for handwashing to decrease bacteria on the skin

Warning

For external use only

Do not use

• in eyes

When using the product

• if in eyes, rinse promptly and thoroughly with water
• discontinue use if irritation and redness develop

Stop use and ask a physician if skin irritation or redness occurs 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

• apply small amont covering hands with product for 30 seconds
• add water, lather, rinse

Other information

• READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
• EMERGENCY HEALTH INFORMATION:1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

INACTIVE INGREDIENT

Inactive ingredients water (aqua), laurtrimonium chloride; cocamidopropyl betaine, cocamidopropyl pg-dimon ium chloride phosphate, PEG-6 cocamide, fragrance, yellow 5, iodopropynyl butylcarbamate, red 33, aloe barbadensis leaf juice, tocopheryl acetate, methylisothiazolinone.

QUESTIONS

Questions? call 1.866.444.7450

Representative label and principal display panel

SWISHER

FOAMING

ANTIBACTERIAL

HAND SOAP TF

6101995

1000 mL (33.8 US FL OZ)

Active ingredient:

Benzalkonium chloride 0.1%

For more ingredient information visit: www.swsh.com

This product may be patented: www.ecolab.com/patents

For questions or comments, call 1-866-444-7450.

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA

© 2019 Ecolab USA Inc. · All rights reserved · Made in U.S.A. · 774104/5400/0119

INGREDIENTS AND APPEARANCE

SWISHER TF 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-601
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-601-26	1000 mL in 1 BAG; Type 0: Not a Combination Product	01/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/15/2019

Labeler - Ecolab Inc. (006154611)