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KANKA
KANKA - 10157-9493-1 - (Benzocaine and Zinc Chloride)
Drug Information of KANKA
| 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) |
Labeler Information of KANKA
| 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 Information of KANKA
| Package NDC: | 10157-9493-1 |
| Package Description: | 1 APPLICATOR in 1 BLISTER PACK (10157-9493-1) > 2 g in 1 APPLICATOR |
NDC Information of KANKA
| 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 |
