NDC 73310-5033

SUN SPR SPF 50

Avobenzone,octinoxate,octocrylene,oxybenzone,titanium Dioxide

SUN SPR SPF 50 is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Agefarm Srl. The primary component is Octinoxate; Octocrylene; Oxybenzone; Titanium Dioxide; Avobenzone.

• Product ID: 73310-5033_92343d88-53cd-48db-e053-2995a90aba7a
• NDC: 73310-5033
• Product Type: Human Otc Drug
• Proprietary Name: SUN SPR SPF 50
• Generic Name: Avobenzone,octinoxate,octocrylene,oxybenzone,titanium Dioxide
• Dosage Form: Spray
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-08-28
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: AGEFARM SRL
• Substance Name: OCTINOXATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE; AVOBENZONE
• Active Ingredient Strength: 1 mg/5mL; mg/5mL; mg/5mL; mg/5mL; mg/5mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 73310-5033-3

150 mL in 1 BOTTLE, SPRAY (73310-5033-3)

• Marketing Start Date: 2019-08-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73310-5033-3 [73310503303]

SUN SPR SPF 50 SPRAY

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-08-28

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	1 mg/5mL

OpenFDA Data

• SPL SET ID: 90d3e398-a822-1608-e053-2a95a90ab318
• Manufacturer:
  • AGEFARM SRL
• UNII:
  • 15FIX9V2JP
  • G63QQF2NOX
  • 95OOS7VE0Y
  • 5A68WGF6WM
  • 4Y5P7MUD51