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Keystone
Keystone - 47593-359-56 - (Benzalkonium Chloride)
Drug Information of Keystone
| Product NDC: | 47593-359 |
| Proprietary Name: | Keystone |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .1 mL/100mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Keystone
| Product NDC: | 47593-359 |
| Labeler Name: | Ecolab Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20020726 |
Package Information of Keystone
| Package NDC: | 47593-359-56 |
| Package Description: | 1200 mL in 1 BOTTLE, PLASTIC (47593-359-56) |
NDC Information of Keystone
| NDC Code | 47593-359-56 |
| Proprietary Name | Keystone |
| Package Description | 1200 mL in 1 BOTTLE, PLASTIC (47593-359-56) |
| Product NDC | 47593-359 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20020726 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ecolab Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
