NDC 14324-013

SUN ULTIMATE FACE SPF 30

Octinoxate, Octisalate, Homosalate, Avobenzone

SUN ULTIMATE FACE SPF 30 is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Naos. The primary component is Octinoxate; Oct.

• Product ID: 14324-013_64434256-5f71-3a23-e053-2991aa0afee2
• NDC: 14324-013
• Product Type: Human Otc Drug
• Proprietary Name: SUN ULTIMATE FACE SPF 30
• Generic Name: Octinoxate, Octisalate, Homosalate, Avobenzone
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-01-31
• Marketing Category: OTC MONOGRAPH N / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: NAOS
• Substance Name: OCTINOXATE; OCT
• Active Ingredient Strength: 70 mg/mL; mg/mL; m
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 14324-013-00

1 BOTTLE in 1 BOX (14324-013-00) > 50 mL in 1 BOTTLE

• Marketing Start Date: 2018-01-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 14324-013-00 [14324001300]

SUN ULTIMATE FACE SPF 30 CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-01-31
• Marketing End Date: 2020-10-31

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	70 mg/mL

OpenFDA Data

• SPL SET ID: 64434256-5f70-3a23-e053-2991aa0afee2
• Manufacturer:
  • NAOS
• UNII:
  • G63QQF2NOX
  • 4X49Y0596W
  • 4Y5P7MUD51
  • V06SV4M95S

NDC Crossover Matching brand name "SUN ULTIMATE FACE SPF 30" or generic name "Octinoxate, Octisalate, Homosalate, Avobenzone"

NDC	Brand Name	Generic Name
14324-013	SUN ULTIMATE FACE SPF 30	OCTINOXATE, OCTISALATE, HOMOSALATE, AVOBENZONE
14324-020	SUN ULTIMATE FACE SPF 30	HOMOSALATE, OCTISALATE, AVOBENZONE