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) |
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 NDC: | 0024-1535-06 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0024-1535-06) |
NDC Code | 0024-1535-06 |
Proprietary Name | Phisohex |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (0024-1535-06) |
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] |