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Trioxin
Trioxin - 68025-041-02 - (Chloroxylenol, Benzocaine and Hydrocortisone Acetate)
Drug Information of Trioxin
| Product NDC: | 68025-041 |
| Proprietary Name: | Trioxin |
| Non Proprietary Name: | Chloroxylenol, Benzocaine and Hydrocortisone Acetate |
| Active Ingredient(s): | 15; 1; 10 mg/mL; mg/mL; mg/mL & nbsp; Chloroxylenol, Benzocaine and Hydrocortisone Acetate |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trioxin
| Product NDC: | 68025-041 |
| Labeler Name: | Vertical Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090702 |
Package Information of Trioxin
| Package NDC: | 68025-041-02 |
| Package Description: | 12 BOTTLE in 1 BOX (68025-041-02) > 2 mL in 1 BOTTLE |
NDC Information of Trioxin
| NDC Code | 68025-041-02 |
| Proprietary Name | Trioxin |
| Package Description | 12 BOTTLE in 1 BOX (68025-041-02) > 2 mL in 1 BOTTLE |
| Product NDC | 68025-041 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chloroxylenol, Benzocaine and Hydrocortisone Acetate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20090702 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Vertical Pharmaceuticals, Inc |
| Substance Name | BENZOCAINE; CHLOROXYLENOL; HYDROCORTISONE ACETATE |
| Strength Number | 15; 1; 10 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
