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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neova DNA Damage Control - Everyday SPF 43 - Drug Facts

Active Ingredients

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

Sunscreen

• Helps prevent sunburn. • Higher SPF gives
more sunburn protection. • Retains SPF after 80 minutes
of activity in the water or perspiring.

Warnings

When using this product

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

Rash or irritation develops and lasts.

Keep out of reach of children

If swallowed, contact a Poison Control Center immediately or get medical help right away.

Directions

• Apply every morning to face, neck
and décolletage. • Reapply as needed or after towel
drying, swimming or perspiring.
• Children under 6 months of age: ask a doctor.

Other Information

High protection sun product.
Sun Alert: Limiting sun exposure, wearing protective
clothing, and using sunscreens may reduce the risks
of skin aging, skin cancer, and other harmful effects
of the sun.
Serious side effects associated with use of this product
may be reported to this number: 888-966-1010.

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 box and label

DNADamageControlEday.jpgLabel DNADConEDAYBox.jpgBox

NEOVA DNA DAMAGE CONTROL - EVERYDAY  SPF 43
zinc oxide, octinoxate, octisalate emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62362-139
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide7.5 mL  in 100 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate7.5 mL  in 100 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate2.5 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Citric Acid (UNII: 2968PHW8QP)  
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)  
Triethoxycaprylylsilane (UNII: LDC331P08E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62362-139-011 in 1 BOX
1NDC:62362-139-7474 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35201/06/2012
Labeler - PhotoMedex, Inc. (054503875)
Establishment
NameAddressID/FEIBusiness Operations
PhotoMedex, Inc.054503875manufacture

Revised: 1/2012
Document Id: 9434e317-85ce-44f4-ac99-dbe37d5f6b6c
Set id: 61c7391c-bc19-4dc3-a3a0-56161da9946d
Version: 1
Effective Time: 20120106
 
PhotoMedex, Inc.