NDC 72839-029

SPF 30 Sunscreen Canisun

Avobenzone 3%, Homosalate 8%, Octisalate 5%, Octocrylene 3%

SPF 30 Sunscreen Canisun is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Derma Care Research Labs, Llc. The primary component is Octisalate; Avobenzone; Homosalate; Octocrylene.

• Product ID: 72839-029_85a4154f-1e43-707f-e053-2a91aa0a2484
• NDC: 72839-029
• Product Type: Human Otc Drug
• Proprietary Name: SPF 30 Sunscreen Canisun
• Generic Name: Avobenzone 3%, Homosalate 8%, Octisalate 5%, Octocrylene 3%
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-06-14
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Derma Care Research Labs, LLC
• Substance Name: OCTISALATE; AVOBENZONE; HOMOSALATE; OCTOCRYLENE
• Active Ingredient Strength: 5 g/100mL; g/100mL; g/100mL; g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72839-029-03

89 mL in 1 TUBE (72839-029-03)

• Marketing Start Date: 2019-06-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72839-029-03 [72839002903]

SPF 30 Sunscreen Canisun LOTION

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-06-14

Drug Details

Active Ingredients

Ingredient	Strength
OCTISALATE	5 g/100mL

OpenFDA Data

• SPL SET ID: 851830de-633c-12a0-e053-2991aa0ac691
• Manufacturer:
  • Derma Care Research Labs, LLC
• UNII:
  • G63QQF2NOX
  • 4X49Y0596W
  • 5A68WGF6WM
  • V06SV4M95S