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Anti Bacterial Foam Hand Problend
Anti Bacterial Foam Hand Problend - 76250-995-02 - (benzalkonium chloride)
Drug Information of Anti Bacterial Foam Hand Problend
| Product NDC: | 76250-995 |
| Proprietary Name: | Anti Bacterial Foam Hand Problend |
| Non Proprietary Name: | benzalkonium chloride |
| Active Ingredient(s): | 1.3 g/1000mL & nbsp; benzalkonium chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti Bacterial Foam Hand Problend
| Product NDC: | 76250-995 |
| Labeler Name: | Seatex Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120531 |
Package Information of Anti Bacterial Foam Hand Problend
| Package NDC: | 76250-995-02 |
| Package Description: | 2 CARTON in 1 CARTON (76250-995-02) > 4 BOTTLE, PLASTIC in 1 CARTON (76250-995-04) > 3780 mL in 1 BOTTLE, PLASTIC (76250-995-01) |
NDC Information of Anti Bacterial Foam Hand Problend
| NDC Code | 76250-995-02 |
| Proprietary Name | Anti Bacterial Foam Hand Problend |
| Package Description | 2 CARTON in 1 CARTON (76250-995-02) > 4 BOTTLE, PLASTIC in 1 CARTON (76250-995-04) > 3780 mL in 1 BOTTLE, PLASTIC (76250-995-01) |
| Product NDC | 76250-995 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzalkonium chloride |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20120531 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Seatex Ltd |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
