NDC 44717-538

Natria Brightening SPF 15

Ethylhexl Methoxycinnamate, Zinc Oxide

Natria Brightening SPF 15 is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Wasatch Product Development. The primary component is Octinoxate; Zinc Oxide.

• Product ID: 44717-538_9412749c-b788-4b7f-8b54-7503da58fb93
• NDC: 44717-538
• Product Type: Human Otc Drug
• Proprietary Name: Natria Brightening SPF 15
• Generic Name: Ethylhexl Methoxycinnamate, Zinc Oxide
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-07-19
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Wasatch Product Development
• Substance Name: OCTINOXATE; ZINC OXIDE
• Active Ingredient Strength: 8 mL/100mL; mL/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 44717-538-02

1 BOTTLE in 1 BOX (44717-538-02) > 50 mL in 1 BOTTLE (44717-538-01)

• Marketing Start Date: 2010-07-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44717-538-02 [44717053802]

Natria Brightening SPF 15 CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-07-19
• Inactivation Date: 2019-10-29

NDC 44717-538-01 [44717053801]

Natria Brightening SPF 15 CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-07-19

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	7.5 mL/100mL

OpenFDA Data

• SPL SET ID: 390d2793-6ee4-44a4-82ae-708bfd039ead
• Manufacturer:
  • Wasatch Product Development
• UNII:
  • SOI2LOH54Z
  • 4Y5P7MUD51