NEOVA DNA DAMAGE CONTROL - ACTIVE BROAD SPECTRUM SPF 43- octinoxate, zinc oxide cream 
PHARMA COSMETICS, INC

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Neova DNA Damage Control Active SPF 43

Active Ingredients

Octinoxate 7.5%, Zinc Oxide 9.0%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not useon damaged or broken skin.

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

Stop use and ask a doctor ifrash occurs.

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

Directions

     °After 80 minutes of swimming or sweating.

     °Immediately after towel drying.

     °At least every two hours.

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

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

Inactive Ingredients

Ascorbyl Palmitate, Butylene Glycol, Citric Acid, Cyclopentasiloxane, Dimethicone, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone/Vinyldimethicone Crosspolymer, Ergothioneine, Ethyl Hexyl Isononanoate,Iodopropynyl Butylcarbamate, Lauryl PEG-9 Polymethylsiloxyethyl Dimethicone, Lecithin, Microcoous Lysate, Phenoxyethanol, Plankton Extract, Purified Water, Retinyl Palmitate, Sodium Chloride, Sodium Hydroxide, Triethanoxycaprylylsilane.

Other Information

Protect this product from excessive heat and direct sun.

Questions or Comments?

Call toll free 1-888-966-1010.

Priduct Label

Neova DNA Damage Control
Active SPF 43
3.0 fl. oz. (89mL)

image description

NEOVA DNA DAMAGE CONTROL - ACTIVE  BROAD SPECTRUM SPF 43
octinoxate, zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72251-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE9 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
ERGOTHIONEINE (UNII: BDZ3DQM98W)  
ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
MICROCOCCUS LUTEUS (UNII: LV6L29Z6AX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72251-003-891 in 1 BOX04/19/2018
189 mL in 1 TUBE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/08/2012
Labeler - PHARMA COSMETICS, INC (080622701)
Establishment
NameAddressID/FEIBusiness Operations
Swiss-American CDMO, LLC080170933manufacture(72251-003)

Revised: 10/2023
Document Id: 075ea91f-7b56-1c8b-e063-6294a90aa765
Set id: 73e8fd63-c992-4e22-bc92-271e34b642ac
Version: 5
Effective Time: 20231010
 
PHARMA COSMETICS, INC