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 – 3 oz. bottle label

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)

Principal Display Panel - Bottle Label
MEDIFIRST ANTISEPTIC 
benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-244
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-244-170.09 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/12/201306/15/2018
2NDC:47682-244-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/14/201505/10/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/29/200905/10/2019
Labeler - Unifirst First Aid Corporation (832947092)
Registrant - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc.874965262manufacture(47682-244)

Revised: 5/2016
Document Id: 05692b4f-b554-4099-adb8-784960255b04
Set id: 7c4270be-e1c5-4354-9a04-0172948baa03
Version: 6
Effective Time: 20160510
 
Unifirst First Aid Corporation