ANTISEPTIC- benzalkonium chloride liquid

Antiseptic by

Drug Labeling and Warnings

Antiseptic by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation, Safetec of America, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium chloride 0.133% w/v

Purpose

First aid antiseptic

Uses

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

For external use only.

Warnings

For external use only

Do not use

• in the eyes or apply over large areas of the body
• longer than 1 week unless directed by a doctor
• in case of deep puncture wounds, animal bites or serious burns, consult a doctor

Stop use and ask doctor if

• the 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

• tear open packet, unfold and clean the affected area
• discard after use
• may be covered with a sterile bandage
• if bandaged, let dry first

Other information

• store at room temperature 59°-86°F (15°-30°C)
• tamper evident sealed packets
• do not use any open or torn packets

Inactive ingredients

alcohol, water

Questions or comments?

1-800-634-7680

Medi-First Label

MEDI-FIRST®

Antiseptic Wipes

Extra Large Wipes

Net Contents: 10 units per box

Product # 21412

INGREDIENTS AND APPEARANCE

ANTISEPTIC 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-214
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: 47682-214-71	20 in 1 BOX	02/22/2012	07/31/2020
1	NDC: 47682-214-99	2.5 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-214-33	100 in 1 BOX	02/22/2012	07/31/2020
2	NDC: 47682-214-99	2.5 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-214-12	10 in 1 BOX	02/22/2012	07/31/2020
3	NDC: 47682-214-99	2.5 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/22/2012	07/31/2020

Labeler - Unifirst First Aid Corporation (832947092)

Registrant - Safetec of America, Inc. (874965262)

Establishment
Name	Address	ID/FEI	Business Operations
Safetec of America, Inc.		874965262	manufacture(47682-214)