Other
Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Quadex Pharmaceuticals, Llc for the product Blister Blaster (NDC 66774-1001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredients, purposes, uses, warning, otc - do not use, otc - stop use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Benzalkonium Chloride 0.13%
Cold Sore/Fever Blister Treatment Topical Antiseptic
Do not use:
Stop use and ask a doctor if:
Ask a doctor if:
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.
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.
Isopropyl alcohol (70% v/v), water.
Questions or to report an adverse event: 1-877-825-7153
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)
* Please review the disclaimer below.