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