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 |