| Product NDC: | 24488-040 |
| Proprietary Name: | KDS Lab |
| Non Proprietary Name: | LIDOCAINE HYDROCHLORIDE, ZINC CHLORIDE, ALCOHOL |
| Active Ingredient(s): | 199.975654; 39.9680796; 400.018936 mg/mL; mg/mL; mg/mL & nbsp; LIDOCAINE HYDROCHLORIDE, ZINC CHLORIDE, ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 24488-040 |
| Labeler Name: | KDS Lab |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121003 |
| Package NDC: | 24488-040-80 |
| Package Description: | 14.786 mL in 1 BOTTLE, DROPPER (24488-040-80) |
| NDC Code | 24488-040-80 |
| Proprietary Name | KDS Lab |
| Package Description | 14.786 mL in 1 BOTTLE, DROPPER (24488-040-80) |
| Product NDC | 24488-040 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | LIDOCAINE HYDROCHLORIDE, ZINC CHLORIDE, ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121003 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | KDS Lab |
| Substance Name | ALCOHOL; LIDOCAINE HYDROCHLORIDE; ZINC CHLORIDE |
| Strength Number | 199.975654; 39.9680796; 400.018936 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |