NEOVA DAY THERAPY SPF 30- homosalate, octocrylene, octisalate, avobenzone lotion

Neova Day Therapy by

Drug Labeling and Warnings

Neova Day Therapy by is a Otc medication manufactured, distributed, or labeled by PHARMA COSMETICS, INC, Northwest Cosmetic Laboratories LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warnings

For external use only. Avoid contact with eyes. If contact
occurs, rinse eyes thoroughly with water. Discontinue use if irritation or
rash appears. Keep out of reach of children. In case of accidental
ingestion, seek professional assistance or contact a Poison Control
Center immediately.

USES

• helps in prevents sunburn
• If used as directed with other sun protection measures
  (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

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

Active Ingredients

Avobenzone 3%, Homosalate 7%, Octisalate 5%,
Octocrylene, 6%.

Inactive Ingredients

Water (Aqua), Isododecane, Hydrogenated Polydecene,
Glycerin, Glyceryl Stearate, Arachidyl Alcohol, Behenyl Alcohol, Bis
(Tripeptide-1) Copper Acetate, Plankton Extract, Triticum Vulgare (Wheat)
Gluten Extract, Glycine Soja (Soybean) Seed Extract, Dimethicone,
Arachidyl Glucoside, Caprylyl Glycol, Xanthan Gum, Cetyl Alcohol,
PEG-100 Stearate, Prunus Armeniaca (Apricot) Kernel Oil, Squalane,
Ammonium Acrylate/Acrylamide Copolymer, Polyisobutene, Polysorbate
20, Sodium Hydroxide, Lecithin, Sodium Chloride, Phenoxyethanol, Sorbic
Acid. May Contain +/- Ultramarines.

Product Label

INGREDIENTS AND APPEARANCE

NEOVA DAY THERAPY  SPF 30
homosalate, octocrylene, octisalate, avobenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72251-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	6 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
DOCOSANOL (UNII: 9G1OE216XY)
PREZATIDE COPPER ACETATE (UNII: A3LEI4P1NB)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
SOYBEAN (UNII: L7HT8F1ZOD)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
ISODODECANE (UNII: A8289P68Y2)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K)
APRICOT KERNEL OIL (UNII: 54JB35T06A)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBIC ACID (UNII: X045WJ989B)
SQUALANE (UNII: GW89575KF9)
WHEAT GERM (UNII: YR3G369F5A)
XANTHAN GUM (UNII: TTV12P4NEE)
ULTRAMARINE BLUE (UNII: I39WR998BI)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	blue (Light Blue)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72251-004-50	1 in 1 BOX	04/12/2018
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	04/12/2018

Labeler - PHARMA COSMETICS, INC (080622701)

Establishment
Name	Address	ID/FEI	Business Operations
Northwest Cosmetic Laboratories LLC		929572014	manufacture(72251-004)