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