NEOVA DNA DAMAGE CONTROL - EVERYDAY BROAD SPECTRUM SPF 44- octinoxate, octisalate, zinc oxide 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]

Active Ingredients

Octinoxate 6.5%, Octisalate 2.5% Zinc Oxide 8.5%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed and with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin again caused by the sun.

Warnings

For external use only

DO NOT USE

Do not use on damaged or broken skin.

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply liberally 15 minutes before sun exposure.
• Use a water resistant sunscreen if swimming or sweating.
• Reapply at least every 2 hours.
• Children under 6 months of age: ask a doctor.
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

      °Limit time in the sun, especially from 10 a.m. - 2 p.m.

      °Wear long-sleeve shirts, pants, hats, and sunglasses.

Inactive Ingredients

Allantoin, Ascorbyl Palmitate, Butylene Glycol, Cetearyl Glucoside, Citric Acid, Cyclopentasiloxane, Dimethicone, Ergothioneine, Ethyl Hexyl Isononanoate, Glycereth-26, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Iodopropynyl Butylcarbamate, Isopropyl Palmitate, Lecithin, Micrococcus Lysate, Octyl Sterate, Oleth-3 Phosphate, Panthenol, PEG-7 Trimethylolprpopane Coconut Ether, Phenoxyethanol, Plankton Extract, Polyether-1, Polyisobutene, Purified Water, Retinyl Palmitate, Sodium Hyaluronate, Sodium Hydroxide, Tocopherol Acetate, Triethoxycaprylysilane.

Other Information

Protect this product from excessive heat and direct sun.

Questions or Comments?

Call toll free 1-888-966-1010.

Neova DNA Damage ControlEveryday SPF 442.5 fl. oz. (74mL) label and box

DNADamageControlEveryday2-5ozLabel.jpg DNADamageControlEveryday2-5ozBox.jpg

INGREDIENTS AND APPEARANCE

NEOVA DNA DAMAGE CONTROL - EVERYDAY  BROAD SPECTRUM SPF 44
octinoxate, octisalate, zinc oxide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62362-159
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	6.5 g  in 100 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	2.5 g  in 100 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	8.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Allantoin (UNII: 344S277G0Z)
Ascorbyl Palmitate (UNII: QN83US2B0N)
Butylene Glycol (UNII: 3XUS85K0RA)
Cetearyl Glucoside (UNII: 09FUA47KNA)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Dimethicone (UNII: 92RU3N3Y1O)
Ergothioneine (UNII: BDZ3DQM98W)
Ethylhexyl Isononanoate (UNII: I6KB4GE3K4)
Glycereth-26 (UNII: NNE56F2N14)
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)
Isopropyl Palmitate (UNII: 8CRQ2TH63M)
Egg Phospholipids (UNII: 1Z74184RGV)
Octyl Stearate (UNII: 772Y4UFC8B)
Oleth-3 Phosphate (UNII: 8Q0Z18J1VL)
Panthenol (UNII: WV9CM0O67Z)
Phenoxyethanol (UNII: HIE492ZZ3T)
Water (UNII: 059QF0KO0R)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Hydroxide (UNII: 55X04QC32I)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Triethoxycaprylylsilane (UNII: LDC331P08E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62362-159-01	1 in 1 BOX
1	NDC: 62362-159-74	74 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	10/08/2012

Labeler - PhotoMedex, Inc. (054503875)

Establishment
Name	Address	ID/FEI	Business Operations
PhotoMedex, Inc.		054503875	manufacture(62362-159)