NDC 65364-218

Sunspray

Avobenzone, Homosalate, Octinoxate, Octisalate, Titanium Dioxide

Sunspray is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Kiss My Face, Llc. The primary component is Avobenzone; Homosalate; Octinoxate; Octisalate; Titanium Dioxide.

• Product ID: 65364-218_c9c86d45-0999-4b7d-81c1-9605fec5192d
• NDC: 65364-218
• Product Type: Human Otc Drug
• Proprietary Name: Sunspray
• Generic Name: Avobenzone, Homosalate, Octinoxate, Octisalate, Titanium Dioxide
• Dosage Form: Spray
• Route of Administration: TOPICAL
• Marketing Start Date: 2015-01-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: Kiss My Face, LLC
• Substance Name: AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
• Active Ingredient Strength: 3 g/100g; g/100g; g/100g; g/100g; g/100g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 65364-218-01

100 g in 1 BOTTLE, SPRAY (65364-218-01)

• Marketing Start Date: 2015-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 65364-218-01 [65364021801]

Sunspray SPRAY

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-01-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
AVOBENZONE	3 g/100g

OpenFDA Data

• SPL SET ID: 5fae3a70-2e9a-44fa-99aa-c905de534144
• Manufacturer:
  • Kiss My Face, LLC
• UNII:
  • 15FIX9V2JP
  • G63QQF2NOX
  • 4X49Y0596W
  • V06SV4M95S
  • 4Y5P7MUD51
• UPC Code:
  • 0028367841982

NDC Crossover Matching brand name "Sunspray" or generic name "Avobenzone, Homosalate, Octinoxate, Octisalate, Titanium Dioxide"

NDC	Brand Name	Generic Name
65364-218	Sunspray	Avobenzone, Homosalate, Octinoxate, Octisalate, Titanium Dioxide
65364-219	Face Factor	Avobenzone, Homosalate, Octinoxate, Octisalate, Titanium Dioxide