ANTISEPTIC- benzalkonium chloride liquid
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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

MF Antiseptic Wipes

ANTISEPTIC
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-214
Route of Administration	TOPICAL

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47682-214-71	20 in 1 BOX	02/22/2012	07/31/2020
1		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		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		2.5 mL in 1 PACKET; Type 0: Not a Combination Product

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

Labeler - Unifirst First Aid Corporation (832947092)

Registrant - Safetec of America, Inc. (874965262)

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

Revised: 6/2020

Document Id: a8e883a8-f3ae-3c24-e053-2a95a90a1650

Set id: 2acfef03-3a0b-44c3-99fe-12aa690f0347

Version: 8

Effective Time: 20200625

Unifirst First Aid Corporation