NDC 62362-139

Neova DNA Damage Control - Everyday SPF 43

Zinc Oxide, Octinoxate, Octisalate

Neova DNA Damage Control - Everyday SPF 43 is a Topical Emulsion in the Human Otc Drug category. It is labeled and distributed by Photomedex, Inc.. The primary component is Zinc Oxide; Octinoxate; Octisalate.

• Product ID: 62362-139_9434e317-85ce-44f4-ac99-dbe37d5f6b6c
• NDC: 62362-139
• Product Type: Human Otc Drug
• Proprietary Name: Neova DNA Damage Control - Everyday SPF 43
• Generic Name: Zinc Oxide, Octinoxate, Octisalate
• Dosage Form: Emulsion
• Route of Administration: TOPICAL
• Marketing Start Date: 2012-01-06
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part352
• Labeler Name: PhotoMedex, Inc.
• Substance Name: ZINC OXIDE; OCTINOXATE; OCTISALATE
• Active Ingredient Strength: 8 mL/100mL; mL/100mL; mL/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 62362-139-03

1 PACKAGE in 1 POUCH (62362-139-03) > 2 mL in 1 PACKAGE (62362-139-02)

• Marketing Start Date: 2012-01-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62362-139-02 [62362013902]

Neova DNA Damage Control - Everyday SPF 43 EMULSION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-01-06

NDC 62362-139-03 [62362013903]

Neova DNA Damage Control - Everyday SPF 43 EMULSION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-01-06
• Inactivation Date: 2019-11-13

NDC 62362-139-01 [62362013901]

Neova DNA Damage Control - Everyday SPF 43 EMULSION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-01-06
• Inactivation Date: 2019-11-13

NDC 62362-139-74 [62362013974]

Neova DNA Damage Control - Everyday SPF 43 EMULSION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-01-06

Drug Details

Active Ingredients

Ingredient	Strength
ZINC OXIDE	7.5 mL/100mL

OpenFDA Data

• SPL SET ID: 77a587f5-d532-405b-91d9-2f0b27c24617
• Manufacturer:
  • PhotoMedex, Inc.
• UNII:
  • SOI2LOH54Z
  • 4X49Y0596W
  • 4Y5P7MUD51

NDC Crossover Matching brand name "Neova DNA Damage Control - Everyday SPF 43" or generic name "Zinc Oxide, Octinoxate, Octisalate"

NDC	Brand Name	Generic Name
13733-019	MISSHA TIME REVOLUTION WHITE CURE UV SUN PROTECTOR	ZINC OXIDE, OCTINOXATE, OCTISALATE
62362-129	Neova DNA Damage Control - Active	Zinc Oxide, Octinoxate, Octisalate
62362-139	Neova DNA Damage Control - Everyday	Zinc Oxide, Octinoxate, Octisalate
51346-439	PROVENCE AIR SKIN FIT PACT 02 NATURAL BEIGE	ZINC OXIDE, OCTINOXATE, OCTISALATE
42521-2930	SkinTx UV Pro Broad Spectrum SPF30	ZINC OXIDE, OCTINOXATE, OCTISALATE
66428-002	TheradermSPF 43	Zinc Oxide, Octinoxate, Octisalate