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MyOxin
MyOxin - 58809-333-15 - (Chloroxylenol, Benzocaine, and Hydrocortisone Acetate)
Drug Information of MyOxin
| Product NDC: | 58809-333 |
| Proprietary Name: | MyOxin |
| 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): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MyOxin
| Product NDC: | 58809-333 |
| Labeler Name: | GM Pharamceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110801 |
Package Information of MyOxin
| Package NDC: | 58809-333-15 |
| Package Description: | 1 BOTTLE, GLASS in 1 BOX (58809-333-15) > 15 mL in 1 BOTTLE, GLASS |
NDC Information of MyOxin
| NDC Code | 58809-333-15 |
| Proprietary Name | MyOxin |
| Package Description | 1 BOTTLE, GLASS in 1 BOX (58809-333-15) > 15 mL in 1 BOTTLE, GLASS |
| Product NDC | 58809-333 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chloroxylenol, Benzocaine, and Hydrocortisone Acetate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | GM Pharamceuticals, 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] |
