Medi-First Antiseptic Spray

Drug Labeling and Warnings

Drug Details [pdf]

MEDIFIRST ANTISEPTIC- benzalkonium chloride spray 
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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Medi-First Antiseptic Spray

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

First Aid Antiseptic

Topical Pain Relief

Uses

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

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

Stop use and ask doctor if condition persists or gets worse

Directions

• clean affected area and 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

alcohol, purified water

Questions or Comments?

1-800-634-7680

PRINCIPAL DISPLAY PANEL – 3 oz. bottle label

MEDI-FIRST

Antiseptic Spray

Pump Spray

Antiseptic

• Treats minor cuts,
  scrapes and
  abrasions
• Helps prevent
  infection

3 FL OZ (90ML)

Principal Display Panel - Bottle Label

MEDI-FIRST ®

Antiseptic Spray

Pump Spray

Antiseptic

• Treats minor cuts,
  scrapes and
  abrasion
• Helps prevent
  infection

2 FL OZ (59.1ML)

MEDIFIRST ANTISEPTIC 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-244
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 g  in 1 L

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: 47682-244-17	0.09 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/12/2013	06/15/2018
2	NDC: 47682-244-02	0.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/14/2015	05/10/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/29/2009	05/10/2019

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(47682-244)

Revised: 5/2016

Document Id: 05692b4f-b554-4099-adb8-784960255b04

Set id: 7c4270be-e1c5-4354-9a04-0172948baa03

Version: 6

Effective Time: 20160510