NEOVA DNA DAMAGE CONTROL - EVERYDAY SPF 43- zinc oxide, octinoxate, octisalate emulsion

Neova DNA Damage Control - Everyday by

Drug Labeling and Warnings

Neova DNA Damage Control - Everyday by is a Otc medication manufactured, distributed, or labeled by PhotoMedex, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use:

Apply every morning to face, neck, décolletage
and hands. Reapply as needed. For optimal results, use daily
with Neova [DNA + Copper] products.

Supplied

in a 2.5 fl. oz. / 74 mL tube.

Active Ingredients:

Zinc Oxide 7.5%, Octinoxate 7.5%, Octisalate 2.5%.

Inactive Ingredients:

Water (Aqua), Isopropyl Palmitate,
Octyl Stearate, Ethyl Hexyl Isononanoate, Cyclopentasiloxane,
Cetearyl Glucoside, Micrococcus Lysate,
Plankton Extract, L-ergothioneine, Dimethicone,
Glycereth-26, Sodium Hyaluronate, Panthenol, Allantoin,
Tocopheryl Acetate, Ascorbyl Palmitate (Vitamin C),
Oleth-3 Phosphate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl
Taurate Copolymer, Polyisobutene, PEG-7
Trimethylolpropane Coconut Ether, Lecithin, Polyether-1,
Phenoxyethanol, Butylene Glycol, Citric Acid, Iodopropynyl
Butylcarbamate, Triethoxycaprylylsilane.

Image of package insert, package, and pouch

PkgInsertUniversalpg1.jpg PkgInsertUniversalpg2.jpg AmpuleEday.jpg PouchEday.jpg

INGREDIENTS AND APPEARANCE

NEOVA DNA DAMAGE CONTROL - EVERYDAY  SPF 43
zinc oxide, octinoxate, octisalate emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62362-139
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	7.5 mL  in 100 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	7.5 mL  in 100 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	2.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isopropyl Palmitate (UNII: 8CRQ2TH63M)
Octyl Stearate (UNII: 772Y4UFC8B)
Ethylhexyl Isononanoate (UNII: I6KB4GE3K4)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Cetearyl Glucoside (UNII: 09FUA47KNA)
Ergothioneine (UNII: BDZ3DQM98W)
Dimethicone (UNII: 92RU3N3Y1O)
Glycereth-26 (UNII: NNE56F2N14)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Panthenol (UNII: WV9CM0O67Z)
Allantoin (UNII: 344S277G0Z)
Alpha-Tocopherol Acetate (UNII: 9E8X80D2L0)
Ascorbyl Palmitate (UNII: QN83US2B0N)
Oleth-3 Phosphate (UNII: 8Q0Z18J1VL)
Polyisobutylene (1300 MW) (UNII: 241BN7J12Y)
Egg Phospholipids (UNII: 1Z74184RGV)
Butylene Glycol (UNII: 3XUS85K0RA)
Citric Acid (UNII: 2968PHW8QP)
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)
Triethoxycaprylylsilane (UNII: LDC331P08E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62362-139-03	1 in 1 POUCH
1	NDC: 62362-139-02	2 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	01/06/2012

Labeler - PhotoMedex, Inc. (054503875)

Establishment
Name	Address	ID/FEI	Business Operations
PhotoMedex, Inc.		054503875	manufacture