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Kank-A
Kank-A - 10157-9477-1 - (Benzocaine)
Drug Information of Kank-A
| Product NDC: | 10157-9477 |
| Proprietary Name: | Kank-A |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 200 mg/mL & nbsp; Benzocaine |
| Administration Route(s): | BUCCAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kank-A
| Product NDC: | 10157-9477 |
| Labeler Name: | Blistex Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111201 |
Package Information of Kank-A
| Package NDC: | 10157-9477-1 |
| Package Description: | 9.75 mL in 1 BOTTLE, WITH APPLICATOR (10157-9477-1) |
NDC Information of Kank-A
| NDC Code | 10157-9477-1 |
| Proprietary Name | Kank-A |
| Package Description | 9.75 mL in 1 BOTTLE, WITH APPLICATOR (10157-9477-1) |
| Product NDC | 10157-9477 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | LIQUID |
| Route Name | BUCCAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blistex Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
