| Product NDC: | 0395-1637 |
| Proprietary Name: | HUMCO Mercuroclear |
| Non Proprietary Name: | Benzalkonium Chloride and Lidocaine Hydrochloride |
| Active Ingredient(s): | 1.3; 25 mg/mL; mg/mL & nbsp; Benzalkonium Chloride and Lidocaine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0395-1637 |
| Labeler Name: | Humco Holding Group, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990225 |
| Package NDC: | 0395-1637-92 |
| Package Description: | 59 mL in 1 BOTTLE (0395-1637-92) |
| NDC Code | 0395-1637-92 |
| Proprietary Name | HUMCO Mercuroclear |
| Package Description | 59 mL in 1 BOTTLE (0395-1637-92) |
| Product NDC | 0395-1637 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride and Lidocaine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 19990225 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Humco Holding Group, Inc |
| Substance Name | BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE |
| Strength Number | 1.3; 25 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |