MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM- benzalkonium chloride liquid

MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM by

Drug Labeling and Warnings

MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM by is a Otc medication manufactured, distributed, or labeled by CARONLAB AUSTRALIA PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic

Uses

• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
• for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame

For external use only

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop
• condition persists 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 hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing

Other information

• store between 15-30°C (59-86°F)
• avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT

Inactive ingredients cocamidopropyl propylene glycol-dimonium chloride phosphate, water

QUESTIONS

Questions? +1-305-985-7803
You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

• decreases bacteria on the skin
• no water required
• non drying

Contains: Benzalkonium Chloride 0.1% w/v

Manufactured by:

Caronlab Australia Pty Ltd

148-150 Victoria St,

North Geelong, VIC, Australia 3215

Product of Australia

www.caronlab.com.au

Phone: + 1-305-985-7803

Made in Australia   Dispose of thoughtfully   Vegan friendly   Certified Cruelty Free

Packaging

INGREDIENTS AND APPEARANCE

MICRO DEFENCE ANTISEPTIC HAND SANITIZER FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77277-633
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77277-633-68	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/30/2020

Labeler - CARONLAB AUSTRALIA PTY LTD (754402154)

Establishment
Name	Address	ID/FEI	Business Operations
CARONLAB AUSTRALIA PTY LTD		754402154	manufacture(77277-633)