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PureForce
PureForce - 47593-496-41 - (Benzalkonium)
Drug Information of PureForce
| Product NDC: | 47593-496 |
| Proprietary Name: | PureForce |
| Non Proprietary Name: | Benzalkonium |
| Active Ingredient(s): | 1 mg/mL & nbsp; Benzalkonium |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PureForce
| Product NDC: | 47593-496 |
| Labeler Name: | Ecolab Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120823 |
Package Information of PureForce
| Package NDC: | 47593-496-41 |
| Package Description: | 750 mL in 1 BOTTLE, PLASTIC (47593-496-41) |
NDC Information of PureForce
| NDC Code | 47593-496-41 |
| Proprietary Name | PureForce |
| Package Description | 750 mL in 1 BOTTLE, PLASTIC (47593-496-41) |
| Product NDC | 47593-496 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120823 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ecolab Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
