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Blister Blaster - 66774-1001-2 - (Benzalkonium chloride)

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Drug Information of Blister Blaster

Product NDC: 66774-1001
Proprietary Name: Blister Blaster
Non Proprietary Name: Benzalkonium chloride
Active Ingredient(s): .12    g/100mL & nbsp;   Benzalkonium chloride
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Blister Blaster

Product NDC: 66774-1001
Labeler Name: Quadex Pharmaceuticals, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100401

Package Information of Blister Blaster

Package NDC: 66774-1001-2
Package Description: 2 VIAL in 1 BLISTER PACK (66774-1001-2) > .6 mL in 1 VIAL

NDC Information of Blister Blaster

NDC Code 66774-1001-2
Proprietary Name Blister Blaster
Package Description 2 VIAL in 1 BLISTER PACK (66774-1001-2) > .6 mL in 1 VIAL
Product NDC 66774-1001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium chloride
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Quadex Pharmaceuticals, LLC
Substance Name BENZALKONIUM CHLORIDE
Strength Number .12
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Blister Blaster


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