MY DAY SCREEN TINTED DROPS MINI 30 SPF LIGHT MEDIUM- zinc oxide, titanium dioxide lotion

My day screen Tinted drops Mini 30 SPF Light Medium by

Drug Labeling and Warnings

My day screen Tinted drops Mini 30 SPF Light Medium by is a Otc medication manufactured, distributed, or labeled by Make2Give LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Zinc Oxide 6%

Titanium Dioxide 6%

Purpose

Sunscreen

Uses

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 Helps prevent sunburn

Warnings

For external use only.

When using this product

• keep out of eyes. Rinse with water to remove.

Stop using and ask a doctor

if a rash or irritation develops and lasts.

Keep out of reach of children.

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

Directions

Apply liberally and spread evenly 15 minutes before sun exposure.

Inactive Ingredients

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Camellia Sinensis (Green Tea) Extract, Caprylic/ Capric Triglyceride, Citric Acid, Citrullus Lanatus (Watermelon) Extract, Cocos Nucifera (Coconut) Oil, Daucus Carota Sativa (Carrot) Extract, Decyl Glucoside, Dodecnate, Ethyl Vanillin, Glycerin, Glyceryl Caprylate, Glyceryl Stearate Citrate, Glyceryl Stearate, Glyceryl Undecylenate, Helianthus Annuus (Sunflower) Oil, Iron Oxides, Lecithin, Mangifera lndica (Mango) Butter, Punica Granatum (Pomegranate) Extract, Saccharide lsomerate, Sodium Citrate, Sodium Polyacrylate, Stearic Acid, Tocopherol (Vitamin E), Xanthan Gum, Zemea (Corn) opanediol, Caramel Color

Other Information

Protect the product from excessive heat and direct sun.

Package Labeling:

INGREDIENTS AND APPEARANCE

MY DAY SCREEN TINTED DROPS MINI 30 SPF LIGHT MEDIUM 
zinc oxide, titanium dioxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75796-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	60 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	60 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
SHEA BUTTER (UNII: K49155WL9Y)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATERMELON (UNII: 231473QB6R)
COCONUT OIL (UNII: Q9L0O73W7L)
CARROT (UNII: L56Z1JK48B)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
DODECANE (UNII: 11A386X1QH)
ETHYL VANILLIN (UNII: YC9ST449YJ)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
FERRIC OXIDE RED (UNII: 1K09F3G675)
MANGO (UNII: I629I3NR86)
PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
SACCHARIDE ISOMERATE (UNII: W8K377W98I)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
STEARIC ACID (UNII: 4ELV7Z65AP)
TOCOPHEROL (UNII: R0ZB2556P8)
XANTHAN GUM (UNII: TTV12P4NEE)
CORN (UNII: 0N8672707O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75796-010-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/01/2023

Labeler - Make2Give LLC (023910159)