Product NDC: | 10157-9493 |
Proprietary Name: | KANKA |
Non Proprietary Name: | Benzocaine and Zinc Chloride |
Active Ingredient(s): | 20; .1 mL/100g; g/100g & nbsp; Benzocaine and Zinc Chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10157-9493 |
Labeler Name: | Blistex Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090501 |
Package NDC: | 10157-9493-1 |
Package Description: | 1 APPLICATOR in 1 BLISTER PACK (10157-9493-1) > 2 g in 1 APPLICATOR |
NDC Code | 10157-9493-1 |
Proprietary Name | KANKA |
Package Description | 1 APPLICATOR in 1 BLISTER PACK (10157-9493-1) > 2 g in 1 APPLICATOR |
Product NDC | 10157-9493 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine and Zinc Chloride |
Dosage Form Name | GEL |
Route Name | ORAL |
Start Marketing Date | 20090501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Blistex Inc. |
Substance Name | BENZOCAINE; ZINC CHLORIDE |
Strength Number | 20; .1 |
Strength Unit | mL/100g; g/100g |
Pharmaceutical Classes |