NDC 58831-2001

EGF UV SHIELD

Oxtinoxate

EGF UV SHIELD is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Dermaesthetics Inc.. The primary component is Octinoxate; Octisalate; Zinc Oxide; Titanium Dioxide; Amiloxate.

• Product ID: 58831-2001_705f9494-f60d-f5fb-e053-2991aa0adda4
• NDC: 58831-2001
• Product Type: Human Otc Drug
• Proprietary Name: EGF UV SHIELD
• Generic Name: Oxtinoxate
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-07-07
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Dermaesthetics Inc.
• Substance Name: OCTINOXATE; OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE; AMILOXATE
• Active Ingredient Strength: 8 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58831-2001-1

60 mL in 1 TUBE (58831-2001-1)

• Marketing Start Date: 2018-07-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58831-2001-1 [58831200101]

EGF UV SHIELD CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-07-07

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	7.5 g/100mL

OpenFDA Data

• SPL SET ID: 705f9494-f60b-f5fb-e053-2991aa0adda4
• Manufacturer:
  • Dermaesthetics Inc.
• UNII:
  • 15FIX9V2JP
  • SOI2LOH54Z
  • 4X49Y0596W
  • 4Y5P7MUD51
  • 376KTP06K8

NDC Crossover Matching brand name "EGF UV SHIELD" or generic name "Oxtinoxate"

NDC	Brand Name	Generic Name
58831-1001	EGF UV SHIELD	OCTINOXATE
58831-2001	EGF UV SHIELD	oxtinoxate