NDC 59886-355

ULTRASOL Sunscreen Lotion SPF 45

Avobenzone, Octinoxate, Octisalate, Oxyybenzone

ULTRASOL Sunscreen Lotion SPF 45 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Fischer Pharmaceuticals Ltd.. The primary component is Avobenzone; Octinoxate; Octisalate; Oxybenzone.

• Product ID: 59886-355_5426e82e-6214-4e8e-a36f-7f83796a1836
• NDC: 59886-355
• Product Type: Human Otc Drug
• Proprietary Name: ULTRASOL Sunscreen Lotion SPF 45
• Generic Name: Avobenzone, Octinoxate, Octisalate, Oxyybenzone
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-09-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Fischer Pharmaceuticals Ltd.
• Substance Name: AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
• Active Ingredient Strength: 2 g/100g; g/100g; g/100g; g/100g
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 59886-355-11

125 g in 1 BOTTLE (59886-355-11)

• Marketing Start Date: 2010-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59886-355-11 [59886035511]

ULTRASOL Sunscreen Lotion SPF 45 LOTION

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
AVOBENZONE	2 g/100g

OpenFDA Data

• SPL SET ID: 624ca1a6-2b56-4511-a83e-08b20aa4045d
• Manufacturer:
  • Fischer Pharmaceuticals Ltd.
• UNII:
  • G63QQF2NOX
  • 95OOS7VE0Y
  • 4X49Y0596W
  • 4Y5P7MUD51