VANOXIDE - 11086-032-11 - (BENZOYL PEROXIDE, HYDROCORTISONE)

Alphabetical Index


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]

Complete Information of VANOXIDE


General Information