MyOxin - Chloroxylenol, Benzocaine, and Hydrocortisone Acetate
Navigation: NDC > Supplier starting with: G > GM PHARAMCEUTICALS, INC| Field | Value |
|---|---|
| NDC Code: | 58809-333 |
| Proprietary Name: | MyOxin |
| Suffix: | |
| Non-Proprietary Name: | Chloroxylenol, Benzocaine, and Hydrocortisone Acetate |
| Dosage Form: | SOLUTION |
| Method: | TOPICAL |
| Original Marketing Date: | 01-08-2011 |
| Category Name: | UNAPPROVED DRUG OTHER |
| Application Number: | |
| Labeler: | GM PHARAMCEUTICALS, INC |
| Substance Name: | BENZOCAINE; CHLOROXYLENOL; HYDROCORTISONE ACETATE |
| Active Numerator Strength: | 15; 1; 10 |
| Active Ingredient Unit: | mg/mL; mg/mL; mg/mL |
| Pharm Classes: | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| DEA Schedule: |