| 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 |