Product NDC: | 49873-019 |
Proprietary Name: | KEEPAN A |
Non Proprietary Name: | benzalkonium chloride, lidocaine hydrochloride |
Active Ingredient(s): | .1; 1 g/100mL; g/100mL & nbsp; benzalkonium chloride, lidocaine hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49873-019 |
Labeler Name: | Sato Pharmaceutical Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19810715 |
Package NDC: | 49873-019-01 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (49873-019-01) > 60 mL in 1 BOTTLE, SPRAY |
NDC Code | 49873-019-01 |
Proprietary Name | KEEPAN A |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (49873-019-01) > 60 mL in 1 BOTTLE, SPRAY |
Product NDC | 49873-019 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzalkonium chloride, lidocaine hydrochloride |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 19810715 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Sato Pharmaceutical Co., Ltd. |
Substance Name | BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE |
Strength Number | .1; 1 |
Strength Unit | g/100mL; g/100mL |
Pharmaceutical Classes |