| Product NDC: | 68776-1006 |
| Proprietary Name: | AFCO 5512 |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | 1.29 mg/mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68776-1006 |
| Labeler Name: | Alex C. Fergusson, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121101 |
| Package NDC: | 68776-1006-3 |
| Package Description: | 208198 mL in 1 DRUM (68776-1006-3) |
| NDC Code | 68776-1006-3 |
| Proprietary Name | AFCO 5512 |
| Package Description | 208198 mL in 1 DRUM (68776-1006-3) |
| Product NDC | 68776-1006 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alex C. Fergusson, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.29 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |