NDC 58443-0129

Ulta SUNSCREEN SPF 45

Octinoxate, Octisalate, Octocrylene, And Oxybenzone

Ulta SUNSCREEN SPF 45 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Prime Enterprises, Inc.. The primary component is Octinoxate; Octisalate; Octocrylene; Oxybenzone.

• Product ID: 58443-0129_7d8a1c4d-e1ab-2a3e-e053-2991aa0a4557
• NDC: 58443-0129
• Product Type: Human Otc Drug
• Proprietary Name: Ulta SUNSCREEN SPF 45
• Generic Name: Octinoxate, Octisalate, Octocrylene, And Oxybenzone
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2007-03-12
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: Prime Enterprises, Inc.
• Substance Name: OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
• Active Ingredient Strength: 71 mg/mL; mg/mL; mg/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58443-0129-4

177 mL in 1 TUBE (58443-0129-4)

• Marketing Start Date: 2007-03-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58443-0129-4 [58443012904]

Ulta SUNSCREEN SPF 45 LOTION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2007-03-12

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	71.25 mg/mL

OpenFDA Data

• SPL SET ID: 9c605e55-5148-4900-902b-f5ce1dbd7bd8
• Manufacturer:
  • Prime Enterprises, Inc.
• UNII:
  • 95OOS7VE0Y
  • 4X49Y0596W
  • 5A68WGF6WM
  • 4Y5P7MUD51