ORMADUS FOODSERVICE ANTIBACTERIAL FOAM- benzalkonium chloride liquid

Ormadus Foodservice Antibacterial Foam by

Drug Labeling and Warnings

Ormadus Foodservice Antibacterial Foam by is a Otc medication manufactured, distributed, or labeled by SC Johnson Professional USA Inc, APEX International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• for hand washing to reduce bacteria on the skin

Warnings

For external use only

Keep out of reach of children and pets.

When using this product

• Avoid contact with eyes.
• In case of contact with eyes, rinse immediately with plenty of water (for at least 10 minutes) and seek medical advise in case of irritation.
• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• How to use: Apply 1 dose (One push) to dry hands.
• Add water and lather hands for 30 seconds.
• Rinse well with running water and dry hands thoroughly.

Inactive ingredients

aqua (water), hexylene glycol, coco-glucoside, cocamidopropyl PG-dimonium chloride phosphate, laurtrimonium chloride, PEG-6 cocamide, citric acid

SPL UNCLASSIFIED SECTION

Distributed by:
Fastenal Company
and its Subsidiaries,
2001 Theurer Blvd.
Winona, MN 55987

PRINCIPAL DISPLAY PANEL - 1 L Cartridge Label

ORMADUS®

Foodservice Antibacterial Foam Soap

Perfume-Free, Dye-Free Antibacterial Foam Hand Wash.
For professional use in food handling and food processing.

Distributed Exlusively by
FASTENAL®

Stock # 0617377
4000010688/DCN9342/03/24

Distributed by:
Fastenal Company
and its Subsidiaries,
2001 Theurer Blvd.
Winona, MN 55987
©2024 fastenal.com
Made in USA with
Globally Sourced Parts

1 L (33.8 fl oz)

INGREDIENTS AND APPEARANCE

ORMADUS FOODSERVICE ANTIBACTERIAL FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
COCO-GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-023-66	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/31/2024

Labeler - SC Johnson Professional USA Inc (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
APEX International, Inc.		015226132	MANUFACTURE(11084-023)