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 |