NDC 11086-032

VANOXIDE HC

Benzoyl Peroxide, Hydrocortisone

VANOXIDE HC is a Topical Lotion in the Human Prescription Drug category. It is labeled and distributed by Summers Laboratories Inc. The primary component is Benzoyl Peroxide; Hydrocortisone.

• Product ID: 11086-032_3d240cdc-51c7-4727-9fc0-ba0c3ce9b282
• NDC: 11086-032
• Product Type: Human Prescription Drug
• Proprietary Name: VANOXIDE HC
• Generic Name: Benzoyl Peroxide, Hydrocortisone
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2009-11-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Summers Laboratories Inc
• Substance Name: BENZOYL PEROXIDE; HYDROCORTISONE
• Active Ingredient Strength: 5 g/100g; g/100g
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 11086-032-01

25 g in 1 BOTTLE (11086-032-01)

• Marketing Start Date: 2009-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 11086-032-01 [11086003201]

VANOXIDE HC LOTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2009-11-01

NDC 11086-032-11 [11086003211]

VANOXIDE HC LOTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-11-01
• Marketing End Date: 2018-11-20

Drug Details

Active Ingredients

Ingredient	Strength
BENZOYL PEROXIDE	5 g/100g

OpenFDA Data

• SPL SET ID: 1f0edbd9-103e-4a49-b7a8-6552ef172c13
• Manufacturer:
  • Summers Laboratories Inc
• UNII:
  • W9WZN9A0GM
  • WI4X0X7BPJ
• RxNorm Concept Unique ID - RxCUI:
  • 244382
  • 211765

Pharmacological Class

• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]
• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]