NDC 71220-012

intense UV protection emulsion

Homosalate, Octinoxate, Octocrylene, Octisalate, And Avobenzone

intense UV protection emulsion is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Innisfree Corporation. The primary component is Homosalate; Octinoxate; Octocrylene; Octisalate; Avobenzone.

• Product ID: 71220-012_b490bf81-f568-1dee-e053-2995a90a3db7
• NDC: 71220-012
• Product Type: Human Otc Drug
• Proprietary Name: intense UV protection emulsion
• Generic Name: Homosalate, Octinoxate, Octocrylene, Octisalate, And Avobenzone
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2017-12-01
• Marketing End Date: 2022-02-03
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: Innisfree Corporation
• Substance Name: HOMOSALATE; OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
• Active Ingredient Strength: 5 g/50mL; g/50mL; g/50mL; g/50mL; g/50mL
• NDC Exclude Flag: N

Packaging

NDC 71220-012-09

1 TUBE in 1 CARTON (71220-012-09) > 50 mL in 1 TUBE

• Marketing Start Date: 2017-12-01
• Marketing End Date: 2022-02-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 71220-012-09 [71220001209]

intense UV protection emulsion LOTION

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-12-01

Drug Details

Active Ingredients

Ingredient	Strength
HOMOSALATE	4.5 g/50mL

OpenFDA Data

• SPL SET ID: 67c5df1a-bdd0-4619-badd-748b444879dc
• Manufacturer:
  • Innisfree Corporation
• UNII:
  • G63QQF2NOX
  • 4X49Y0596W
  • 5A68WGF6WM
  • V06SV4M95S
  • 4Y5P7MUD51