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GenRx All Purpose Cleansing
GenRx All Purpose Cleansing - 59088-543-16 - (Benzalkonium Chloride)
Drug Information of GenRx All Purpose Cleansing
| Product NDC: | 59088-543 |
| Proprietary Name: | GenRx All Purpose Cleansing |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | 1.3 mg/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GenRx All Purpose Cleansing
| Product NDC: | 59088-543 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130108 |
Package Information of GenRx All Purpose Cleansing
| Package NDC: | 59088-543-16 |
| Package Description: | 237 mL in 1 BOTTLE, SPRAY (59088-543-16) |
NDC Information of GenRx All Purpose Cleansing
| NDC Code | 59088-543-16 |
| Proprietary Name | GenRx All Purpose Cleansing |
| Package Description | 237 mL in 1 BOTTLE, SPRAY (59088-543-16) |
| Product NDC | 59088-543 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20130108 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PureTek Corporation |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
