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Phisohex
Phisohex - 0024-1535-02 - (hexachlorophene)
Drug Information of Phisohex
| Product NDC: | 0024-1535 |
| Proprietary Name: | Phisohex |
| Non Proprietary Name: | hexachlorophene |
| Active Ingredient(s): | 30 mg/mL & nbsp; hexachlorophene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phisohex
| Product NDC: | 0024-1535 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA006882 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19760611 |
Package Information of Phisohex
| Package NDC: | 0024-1535-02 |
| Package Description: | 148 mL in 1 BOTTLE, PLASTIC (0024-1535-02) |
NDC Information of Phisohex
| NDC Code | 0024-1535-02 |
| Proprietary Name | Phisohex |
| Package Description | 148 mL in 1 BOTTLE, PLASTIC (0024-1535-02) |
| Product NDC | 0024-1535 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hexachlorophene |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 19760611 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | HEXACHLOROPHENE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antiseptic [EPC] |
