NDC 55118-600

Sunscreen Mango and Coconut

Avobenzone, Octinoxate, Octisalate, Octocrylene, And Oxybenzone

Sunscreen Mango and Coconut is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Kimberly-clark Corporation. The primary component is Avobenzone; Octinoxate; Octisalate; Octocrylene; Oxybenzone.

• Product ID: 55118-600_858ce55b-2916-4778-bbfd-9e88cbb81c11
• NDC: 55118-600
• Product Type: Human Otc Drug
• Proprietary Name: Sunscreen Mango and Coconut
• Generic Name: Avobenzone, Octinoxate, Octisalate, Octocrylene, And Oxybenzone
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-03-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Kimberly-Clark Corporation
• Substance Name: AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
• Active Ingredient Strength: 10 mg/g; mg/g; mg/g; mg/g; mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 55118-600-11

45 g in 1 BOTTLE, PLASTIC (55118-600-11)

• Marketing Start Date: 2010-03-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55118-600-11 [55118060011]

Sunscreen Mango and Coconut LOTION

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-03-15
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
AVOBENZONE	10 mg/g

OpenFDA Data

• SPL SET ID: aff60363-62f7-476c-accb-032e28e82793
• Manufacturer:
  • Kimberly-Clark Corporation
• UNII:
  • G63QQF2NOX
  • 95OOS7VE0Y
  • 4X49Y0596W
  • 5A68WGF6WM
  • 4Y5P7MUD51