NDC 72370-0001

Solco platino plus uv sun

Ethylhexyl Methoxycinnamate, Zinc Oxide, Ethylhexyl Salicylate, Titanium Dioxide, Octocrylene

Solco platino plus uv sun is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Solco Biomedical Co., Ltd.. The primary component is Zinc Oxide; Titanium Dioxide; Octinoxate; Octocrylene; Octisalate.

• Product ID: 72370-0001_6ea482e3-9e9d-4eea-e053-2991aa0a042a
• NDC: 72370-0001
• Product Type: Human Otc Drug
• Proprietary Name: Solco platino plus uv sun
• Generic Name: Ethylhexyl Methoxycinnamate, Zinc Oxide, Ethylhexyl Salicylate, Titanium Dioxide, Octocrylene
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-06-12
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: SOLCO BIOMEDICAL CO., LTD.
• Substance Name: ZINC OXIDE; TITANIUM DIOXIDE; OCTINOXATE; OCTOCRYLENE; OCTISALATE
• Active Ingredient Strength: 7 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 72370-0001-1

60 mL in 1 TUBE (72370-0001-1)

• Marketing Start Date: 2018-06-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72370-0001-1 [72370000101]

Solco platino plus uv sun CREAM

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-06-12
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ZINC OXIDE	7.275 g/100mL

OpenFDA Data

• SPL SET ID: 0948a053-5059-4205-a649-6215b2051f05
• Manufacturer:
  • SOLCO BIOMEDICAL CO., LTD.
• UNII:
  • 15FIX9V2JP
  • SOI2LOH54Z
  • 4X49Y0596W
  • 5A68WGF6WM
  • 4Y5P7MUD51