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Antibacterial Foam
Antibacterial Foam - 51053-501-10 - (Chloroxylenol)
Drug Information of Antibacterial Foam
| Product NDC: | 51053-501 |
| Proprietary Name: | Antibacterial Foam |
| Non Proprietary Name: | Chloroxylenol |
| Active Ingredient(s): | 5 mL/1000mL & nbsp; Chloroxylenol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antibacterial Foam
| Product NDC: | 51053-501 |
| Labeler Name: | Sanihealth Products Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100518 |
Package Information of Antibacterial Foam
| Package NDC: | 51053-501-10 |
| Package Description: | 1 BOTTLE, PUMP in 1 BOX (51053-501-10) > 1000 mL in 1 BOTTLE, PUMP |
NDC Information of Antibacterial Foam
| NDC Code | 51053-501-10 |
| Proprietary Name | Antibacterial Foam |
| Package Description | 1 BOTTLE, PUMP in 1 BOX (51053-501-10) > 1000 mL in 1 BOTTLE, PUMP |
| Product NDC | 51053-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chloroxylenol |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20100518 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Sanihealth Products Corporation |
| Substance Name | CHLOROXYLENOL |
| Strength Number | 5 |
| Strength Unit | mL/1000mL |
| Pharmaceutical Classes |
