DAY DAILY ANTI-AGING MOISTURIZING FACE BROAD SPECTRUM SPF 20 SUNSCREEN- zinc oxide, octinoxate cream

DAY Daily Anti-Aging Moisturizing Face Broad Spectrum SPF 20 Sunscreen by

Drug Labeling and Warnings

DAY Daily Anti-Aging Moisturizing Face Broad Spectrum SPF 20 Sunscreen by is a Otc medication manufactured, distributed, or labeled by IDLife, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Zinc Oxide 5.0%, Octinoxate 7.5%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• Higher SPF gives more sunburn protection.
• If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

• ​For external use only

Do not use on

damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs.

Keep out of the reach of children.

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

Directions

For sunscreen use:

• Apply liberally 15 minutes before sun exposure.
• Use a water resistant sunscreen if swimming or sweating.
• Reapply at least every two hours.
• Children under 6 months: 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-sleeved shirts, pants, hats, and sunglasses.

Other Information

• Protect this product from excessive heat and direct sun.

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetearyl Glucoside, Cetyl Esters, Cichorium Intybus (Chicory) Root Extract, Citrullus Lanatus (Watermelon) Fruit Extract, Coco-Caprylate /Caprate, Dimethicone, Dipotassium Glycyrrhizinate, Ethylhexylglycerin, Ethyl Linoleate, Glycerin, Glyceryl Stearate SE, Hydrolyzed Soybean Fiber, lsopropyl Palmitate, Kappaphycus Alvarezii Extract, Lens Esculenta (Lentil) Fruit Extract, Panthenol, Phenoxyethanol, Pyrus Malus (Apple)Fruit Extract, Sclerotium Gum, Shorea Stenoptera Seed Butter, Sodium Lactate, Sodium PCA, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Tropaeolum Majus Flower/Leaf/Stem Extract, Xanthan Gum

Questions?

Visit www.idlife.com or call toll free 855-987-4430

Product Label

INGREDIENTS AND APPEARANCE

DAY DAILY ANTI-AGING MOISTURIZING FACE BROAD SPECTRUM SPF 20 SUNSCREEN 
zinc oxide, octinoxate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70068-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	50 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SHEANUT OIL (UNII: O88E196QRF)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
CETYL ESTERS WAX (UNII: D072FFP9GU)
CHICORY ROOT (UNII: 090CTY533N)
COCO-CAPRYLATE (UNII: 4828G836N6)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
KAPPAPHYCUS ALVAREZII (UNII: T479H08K2O)
PANTHENOL (UNII: WV9CM0O67Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
SHOREA STENOPTERA SEED BUTTER (UNII: 129R0X862G)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROPAEOLUM MAJUS FLOWERING TOP (UNII: RGT30824HY)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70068-001-01	1 in 1 BOX	08/26/2015
1		44.5 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	08/26/2015

Labeler - IDLife, LLC (051244896)