GREEN GUARD FIRST AID ANTISEPTIC- benzalkonium chloride spray

GREEN GUARD First Aid Antiseptic by

Drug Labeling and Warnings

GREEN GUARD First Aid Antiseptic by is a Otc medication manufactured, distributed, or labeled by Ultra Distributors Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

First aid antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes & burns

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

• near eyes or mucous membranes
• on deep or puncture wounds, animal bites, or serious burns
• over large areas of the body
• more than one week unless directed by a doctor

Stop use and ask a doctor

if condition persists or gets worse

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• clean affected area & spray 1 to 3 times daily
• may be covered with a sterile bandage
• not to be used on children under 12 years of age

Inactive ingredients

ethyl alcohol, purified water

Questions or comments?

1-800-869-6970

SPL UNCLASSIFIED SECTION

Treats minor cuts, scrapes and abrasions

Helps prevent infection

Store at 68°-77°F (20°-25°C)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GREEN GUARD FIRST AID ANTISEPTIC 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78495-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78495-112-01	59.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/19/2020

Labeler - Ultra Distributors Inc (007160073)