BLISTER BLASTER- benzalkonium chloride liquid 
Quadex Pharmaceuticals, LLC

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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blisterblaster®

Drug Facts

Active ingredients

Benzalkonium Chloride 0.13%

Purposes

Cold Sore/Fever Blister Treatment Topical Antiseptic

Uses

Warning

Do not use:

  • in the eyes.
  • over large areas of the body.
  • longer than one week unless directed by a doctor.
  • more than 3 times per day.
  • if you are allergic to any ingredient in this product.

Stop use and ask a doctor if:

  • condition persists or worsens.
  • symptoms persist for more than 7 days.

Ask a doctor if:

  • used to treat deep or puncture wounds, animal bites, or serious burns.
  • you are pregnant or nursing a baby.

When using this product you may feel a brief stinging sensation when you apply it. The sting should go away in a short time.

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

Directions - Adults and children over 2 years of age

Other information

Store at room temperature. The ingredients in toothpaste, soft drinks, and some fruit juices can deactivate the active ingredient in Blister Blaster. For best results, avoid brushing your teeth with toothpaste or drinking soft drinks or fruit juices for at least one hour after applying the drug.

Inactive ingredients

Isopropyl alcohol (70% v/v), water.

Questions or to report an adverse event: 1-877-825-7153

PRINCIPAL DISPLAY PANEL - 0.6 ml Vial Blister Pack

NDC 66774-1001-2

blisterblaster®

One Day,
One Dose,
Healing Begins.

Finally, a cold sore treatment that actually
works—so you can clear away that THING
on your lip right now!

Relieves Pain and Burning

Not available through retail stores; avoid imitations.

Contents: 2 Vials (0.6 ml)

PRINCIPAL DISPLAY PANEL - 0.6 ml Vial Blister Pack
BLISTER BLASTER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66774-1001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium chloride0.12 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Isopropyl Alcohol (UNII: ND2M416302) 70 mL  in 100 mL
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66774-1001-22 in 1 BLISTER PACK
10.6 mL in 1 VIAL
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A04/01/2010
Labeler - Quadex Pharmaceuticals, LLC (090438909)
Establishment
NameAddressID/FEIBusiness Operations
James Alexander Corporation040756421MANUFACTURE

Revised: 7/2011
Document Id: 06ab05e1-e358-4cfe-b092-e5eacf629918
Set id: 3481c8f5-6efe-4e57-b562-50385262f47b
Version: 1
Effective Time: 20110708
 
Quadex Pharmaceuticals, LLC