NDC 54272-201

BRIGHTEN SPF 30

Zinc Oxide Octinoxate

BRIGHTEN SPF 30 is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Cen Beauty Llc. The primary component is Zinc Oxide; Octinoxate.

• Product ID: 54272-201_ec0b39fc-fb2a-4269-b9c8-77deed734b95
• NDC: 54272-201
• Product Type: Human Otc Drug
• Proprietary Name: BRIGHTEN SPF 30
• Generic Name: Zinc Oxide Octinoxate
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-02-21
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: CEN BEAUTY LLC
• Substance Name: ZINC OXIDE; OCTINOXATE
• Active Ingredient Strength: 15 g/100mL; g/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 54272-201-11

30 mL in 1 TUBE (54272-201-11)

• Marketing Start Date: 2013-02-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54272-201-11 [54272020111]

BRIGHTEN SPF 30 CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-02-21
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
ZINC OXIDE	15 g/100mL

OpenFDA Data

• SPL SET ID: d5c19a00-c110-4fa5-8573-bbdf3c52fab5
• Manufacturer:
  • CEN BEAUTY LLC
• UNII:
  • SOI2LOH54Z
  • 4Y5P7MUD51

NDC Crossover Matching brand name "BRIGHTEN SPF 30" or generic name "Zinc Oxide Octinoxate"

NDC	Brand Name	Generic Name
54272-201	BRIGHTEN	ZINC OXIDE OCTINOXATE
54272-202	FIRMING DAY	ZINC OXIDE OCTINOXATE