NDC 51350-005

Relovox

Renewing Clarifying Cleanser

Relovox is a Topical Emulsion in the Human Otc Drug category. It is labeled and distributed by Transdermal Corp. The primary component is Benzoyl Peroxide.

• Product ID: 51350-005_ded8ab1d-4ff4-422e-95e5-0582e06888e4
• NDC: 51350-005
• Product Type: Human Otc Drug
• Proprietary Name: Relovox
• Generic Name: Renewing Clarifying Cleanser
• Dosage Form: Emulsion
• Route of Administration: TOPICAL
• Marketing Start Date: 2011-03-31
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333D
• Labeler Name: Transdermal Corp
• Substance Name: BENZOYL PEROXIDE
• Active Ingredient Strength: 25 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51350-005-06

1 TUBE in 1 CARTON (51350-005-06) > 30 g in 1 TUBE (51350-005-05)

• Marketing Start Date: 2011-03-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51350-005-06 [51350000506]

Relovox EMULSION

• Marketing Category: OTC monograph not final
• Application Number: part333D
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-03-31
• Inactivation Date: 2019-10-29

NDC 51350-005-05 [51350000505]

Relovox EMULSION

• Marketing Category: OTC monograph not final
• Application Number: part333D
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-03-31

Drug Details

Active Ingredients

Ingredient	Strength
BENZOYL PEROXIDE	25 mg/g

OpenFDA Data

• SPL SET ID: ee049b13-d15a-495f-9c95-3f28c4161dae
• Manufacturer:
  • Transdermal Corp
• UNII:
  • W9WZN9A0GM
• RxNorm Concept Unique ID - RxCUI:
  • 1094744
  • 845836