FIRST AID- benzalkonium chloride, benzocaine spray

First Aid by

Drug Labeling and Warnings

First Aid by is a Otc medication manufactured, distributed, or labeled by HART Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzalkonium Chloride 0.1%

Benzocaine 5.0%

Purpose

Topical Antiseptic

Topical Anethetic

Uses

First aid to help protect against skin infection and for the temporary relief of pain and itching in

• minor cuts and scrapes
• bites
• skin irritation

Warnings

For external use only.

Flammable, keep away from heat or flame

DO NOT USE

Do not use

• in or near the eyes
• over large portions of the body
• in large quantities, particularly over raw surfaces or blistered areas
• on deep or puncture wounds
• on animal bites
• on serious burns
• longer than 7 days unless directed by a doctor

STOP USE

Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 1-800-222-1222

Directions

• clean affected area and spray 1 to 3 times daily
• may be covered with a sterile bandage

Children under 2 years of age: ask a doctor

Inactive Ingredients

Isopropyl Alcohol, Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIRST AID 
benzalkonium chloride, benzocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50332-0212
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.001 mg  in 1 mg
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	.05 mg  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50332-0212-1	60 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/06/1996

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/06/1996

Labeler - HART Health (069560969)