NDC 51523-675

FACE IT AURA COLOR CONTROL 32800675

Octinoxate, Titanium Oxide And Zinc Oxide

FACE IT AURA COLOR CONTROL 32800675 is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Thefaceshop Co., Ltd.. The primary component is Titanium Dioxide; Zinc Oxide; Octinoxate.

• Product ID: 51523-675_08121399-0956-4b48-e054-00144ff88e88
• NDC: 51523-675
• Product Type: Human Otc Drug
• Proprietary Name: FACE IT AURA COLOR CONTROL 32800675
• Generic Name: Octinoxate, Titanium Oxide And Zinc Oxide
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-11-20
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: THEFACESHOP CO., LTD.
• Substance Name: TITANIUM DIOXIDE; ZINC OXIDE; OCTINOXATE
• Active Ingredient Strength: 2 g/20g; g/20g; g/20g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51523-675-19

1 CONTAINER in 1 CARTON (51523-675-19) > 20 g in 1 CONTAINER

• Marketing Start Date: 2014-11-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51523-675-19 [51523067519]

FACE IT AURA COLOR CONTROL 32800675 CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-11-20
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
TITANIUM DIOXIDE	2.3 g/20g

OpenFDA Data

• SPL SET ID: 08121399-0955-4b48-e054-00144ff88e88
• Manufacturer:
  • THEFACESHOP CO., LTD.
• UNII:
  • 15FIX9V2JP
  • SOI2LOH54Z
  • 4Y5P7MUD51

NDC Crossover Matching brand name "FACE IT AURA COLOR CONTROL 32800675" or generic name "Octinoxate, Titanium Oxide And Zinc Oxide"

NDC	Brand Name	Generic Name
51523-658	FACE IT AURA COLOR CONTROL	octinoxate, titanium oxide and zinc oxide
51523-675	FACE IT AURA COLOR CONTROL	octinoxate, titanium oxide and zinc oxide