E L F WHOA GLOW BROAD SPECTRUM SPF 30 SUNSCREEN SHEER BRONZE SHIMMER SUNBURST- avobenzone, homosalate, octisalate, octocrylene cream

e l f Whoa Glow Broad Spectrum SPF 30 Sunscreen Sheer Bronze Shimmer Sunburst by

Drug Labeling and Warnings

e l f Whoa Glow Broad Spectrum SPF 30 Sunscreen Sheer Bronze Shimmer Sunburst 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 Ingredients

Avobenzone 3.0%

Homosalate 7.3%

Octisalate 4.0%

Octocrylene 8.5%

Purpose

Sunscreen

Use

• Helps prevent 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.

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 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 10 a.m.-2 p.m., wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months of age: ask a doctor

Other Information

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

Inactive Ingredients

Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Niacinamide, Synthetic Fluorphogopite, Trehalose, Stearyl Heptanoate, Silica, Aloe Barbadensis Leaf Juice, Panthenol, Squalane, Sodium Hyaluronate, Caprylyl Glycol, Ethylhexylglycerin, Cetearyl Alcohol, Palmitic Acid, Cetearyl Olivate, Stearic Acid, Sorbitan Olivate, Polyacrylate-13, Glyceryl Stearate Citrate, Polyisobutene, Dimethicone, Polysorbate 20, Sorbitan Isostearate, Potassium Sorbate, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Mica, Phenoxyethanol, Citric Acid, Disodium EDTA, Sodium Benzoate May Contain:Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77499), Yellow 5 (CI 19140)

Questions or comments?

1-888-315-9814

Package labelling:

INGREDIENTS AND APPEARANCE

E L F WHOA GLOW BROAD SPECTRUM SPF 30 SUNSCREEN SHEER BRONZE SHIMMER SUNBURST 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-451
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	73 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	40 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	85 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
NIACINAMIDE (UNII: 25X51I8RD4)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
TREHALOSE (UNII: B8WCK70T7I)
STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PANTHENOL (UNII: WV9CM0O67Z)
SQUALANE (UNII: GW89575KF9)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PALMITIC ACID (UNII: 2V16EO95H1)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN OLIVATE (UNII: MDL271E3GR)
POLYACRYLATE-13 (UNII: FS2D4T67EA)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
MICA (UNII: V8A1AW0880)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-451-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	07/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/20/2024

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