WELL PEOPLE DAYGLEAMER LIQUID MINERAL SUNSCREEN SPF 34- zinc oxide lotion

Well People Daygleamer Liquid Mineral Sunscreen SPF 34 by

Drug Labeling and Warnings

Well People Daygleamer Liquid Mineral Sunscreen SPF 34 by is a Otc medication manufactured, distributed, or labeled by e.l.f. Cosmetics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Zinc Oxide 14.28%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging.

ACTIVE INGREDIENT

Zinc Oxide 14.28%

Warning

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 reach of children

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

Directions

• Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours.
• Use water resistant sunscreen if swimming or sweating.
• 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 value of 15 or higher and other sun protection measures including: limit time in sun, especially from 10a.m.-2 p.m., wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months of age: ask a doctor.

Other Information

Protect this product in this container from excessive heat and direct sun.

Inactive Ingredients

Water (Aqua), Caprylic/Capric Triglyceride, Propanediol, Coco-Caprylate/Caprate, Dicaprylyl Carbonate, Argania Spinosa Kernel Oil, Niacinamide, Squalane, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, 1,2-Hexanediol, Cetearyl Olivate, Sorbitan Olivate, Cetyl Alcohol, Hydroxyacetophenone, Panthenol, Tocopherol, Xanthan Gum, Sorbitan Oleate Decylglucoside Crosspolymer, Butylene Glycol, Isostearic Acid, Lecithin, Polyglyceryl-3 Polyricinoleate, Polyhydroxystearic Acid, Bisabolol, Tetrahexyldecyl Ascorbate, Canola Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Aurantifolia (Lime) Oil, Biosaccharide Gum-4, Altermonas Ferment Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Limon (Lemon) Peel Oil, Zingiber Officale (Ginger) Root Oil, Citric Acid, Potassium Sorbate, Sodium Benzoate, Humulus Lupulus (Hops) Strobile, Farnesol, Limonene

Questions or Comments?

1-888-315-9814

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WELL PEOPLE DAYGLEAMER LIQUID MINERAL SUNSCREEN SPF 34 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	142.8 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BISABOLOL (UNII: 24WE03BX2T)
CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL (UNII: AKN3KSD11B)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PANTHENOL (UNII: WV9CM0O67Z)
XANTHAN GUM (UNII: TTV12P4NEE)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
CITRIC ACID (UNII: 2968PHW8QP)
FARNESOL (UNII: EB41QIU6JL)
LIMONENE, (-)- (UNII: 47MAJ1Y2NE)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CETYL ALCOHOL (UNII: 936JST6JCN)
CANOLA OIL (UNII: 331KBJ17RK)
CITRUS AURANTIFOLIA (LIME) OIL (UNII: UZH29XGA8G)
BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPANEDIOL (UNII: 5965N8W85T)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
WATER (UNII: 059QF0KO0R)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ISOSTEARIC ACID (UNII: X33R8U0062)
CITRUS LIMON (LEMON) PEEL OIL (UNII: I9GRO824LL)
ZINGIBER OFFICINALE (GINGER) ROOT OIL (UNII: SAS9Z1SVUK)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
SQUALANE (UNII: GW89575KF9)
SORBITAN OLEATE DECYLGLUCOSIDE CROSSPOLYMER (UNII: XF9DUA7ABU)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)
ARGANIA SPINOSA KERNEL OIL (UNII: 4V59G5UW9X)
NIACINAMIDE (UNII: 25X51I8RD4)
TOCOPHEROL (UNII: R0ZB2556P8)
ALTEROMONAS MACLEODII (UNII: BPX036043D)
HOPS (UNII: 01G73H6H83)
CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL (UNII: 39W1PKE3JI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-020-01	1 in 1 CARTON	02/13/2025
1		50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/13/2025

Labeler - e.l.f. Cosmetics, Inc. (093902816)