Product NDC: | 24286-1553 |
Proprietary Name: | De La Cruz Mercurochrome |
Non Proprietary Name: | BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE |
Active Ingredient(s): | .13; 2.5 mL/100mL; mL/100mL & nbsp; BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24286-1553 |
Labeler Name: | DLC Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110630 |
Package NDC: | 24286-1553-1 |
Package Description: | 30 mL in 1 BOTTLE (24286-1553-1) |
NDC Code | 24286-1553-1 |
Proprietary Name | De La Cruz Mercurochrome |
Package Description | 30 mL in 1 BOTTLE (24286-1553-1) |
Product NDC | 24286-1553 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110630 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DLC Laboratories, Inc. |
Substance Name | BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE |
Strength Number | .13; 2.5 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |