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ANTIBACTERIAL FOAMING
ANTIBACTERIAL FOAMING - 37808-177-32 - (TRICLOSAN)
Drug Information of ANTIBACTERIAL FOAMING
| Product NDC: | 37808-177 |
| Proprietary Name: | ANTIBACTERIAL FOAMING |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .46 mL/100mL & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANTIBACTERIAL FOAMING
| Product NDC: | 37808-177 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110909 |
Package Information of ANTIBACTERIAL FOAMING
| Package NDC: | 37808-177-32 |
| Package Description: | 946 mL in 1 BOTTLE (37808-177-32) |
NDC Information of ANTIBACTERIAL FOAMING
| NDC Code | 37808-177-32 |
| Proprietary Name | ANTIBACTERIAL FOAMING |
| Package Description | 946 mL in 1 BOTTLE (37808-177-32) |
| Product NDC | 37808-177 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110909 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| Substance Name | TRICLOSAN |
| Strength Number | .46 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
