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VANOXIDE
VANOXIDE - 11086-032-11 - (BENZOYL PEROXIDE, HYDROCORTISONE)
Drug Information of VANOXIDE
| Product NDC: | 11086-032 |
| Proprietary Name: | VANOXIDE |
| Non Proprietary Name: | BENZOYL PEROXIDE, HYDROCORTISONE |
| Active Ingredient(s): | 5; .5 g/100g; g/100g & nbsp; BENZOYL PEROXIDE, HYDROCORTISONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VANOXIDE
| Product NDC: | 11086-032 |
| Labeler Name: | Summers Laboratories Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091101 |
Package Information of VANOXIDE
| Package NDC: | 11086-032-11 |
| Package Description: | 1 BOTTLE in 1 BOX (11086-032-11) > 25 g in 1 BOTTLE (11086-032-01) |
NDC Information of VANOXIDE
| NDC Code | 11086-032-11 |
| Proprietary Name | VANOXIDE |
| Package Description | 1 BOTTLE in 1 BOX (11086-032-11) > 25 g in 1 BOTTLE (11086-032-01) |
| Product NDC | 11086-032 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BENZOYL PEROXIDE, HYDROCORTISONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Summers Laboratories Inc |
| Substance Name | BENZOYL PEROXIDE; HYDROCORTISONE |
| Strength Number | 5; .5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
