NDC 62362-129

Neova DNA Damage Control - Active SPF 45

Zinc Oxide, Octinoxate, Octisalate

Neova DNA Damage Control - Active SPF 45 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: 62362-129_657c11fe-04b0-46aa-bbbd-6b740934f08c
• NDC: 62362-129
• Product Type: Human Otc Drug
• Proprietary Name: Neova DNA Damage Control - Active SPF 45
• 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 62362-129-01

1 TUBE in 1 BOX (62362-129-01) > 89 mL in 1 TUBE (62362-129-89)

• Marketing Start Date: 2012-01-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62362-129-03 [62362012903]

Neova DNA Damage Control - Active SPF 45 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 62362-129-02 [62362012902]

Neova DNA Damage Control - Active SPF 45 EMULSION

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

NDC 62362-129-89 [62362012989]

Neova DNA Damage Control - Active SPF 45 EMULSION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-01-05

NDC 62362-129-01 [62362012901]

Neova DNA Damage Control - Active SPF 45 EMULSION

• Marketing Category: OTC monograph final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-01-05
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
ZINC OXIDE	8 mL/100mL

OpenFDA Data

• SPL SET ID: d2e404d0-2d91-485a-a1ac-d109f96603ce
• Manufacturer:
  • PhotoMedex, Inc.
• UNII:
  • SOI2LOH54Z
  • 4X49Y0596W
  • 4Y5P7MUD51

NDC Crossover Matching brand name "Neova DNA Damage Control - Active SPF 45" 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