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Bacti-Foam
Bacti-Foam - 47593-169-56 - (Triclosan)
Drug Information of Bacti-Foam
| Product NDC: | 47593-169 |
| Proprietary Name: | Bacti-Foam |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | 3 mg/mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bacti-Foam
| Product NDC: | 47593-169 |
| Labeler Name: | Ecolab Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19970711 |
Package Information of Bacti-Foam
| Package NDC: | 47593-169-56 |
| Package Description: | 1200 mL in 1 BOTTLE, PLASTIC (47593-169-56) |
NDC Information of Bacti-Foam
| NDC Code | 47593-169-56 |
| Proprietary Name | Bacti-Foam |
| Package Description | 1200 mL in 1 BOTTLE, PLASTIC (47593-169-56) |
| Product NDC | 47593-169 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19970711 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ecolab Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
