e.l.f Whoa Glow Broad Spectrum SPF30 Sunscreen

e.l.f Whoa Glow Broad Spectrum SPF30 Sunscreen by

Drug Labeling and Warnings

e.l.f Whoa Glow Broad Spectrum SPF30 Sunscreen by is a Otc medication manufactured, distributed, or labeled by e.l.f. Cosmetics, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

E.L.F WHOA GLOW BROAD SPECTRUM SPF30 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene cream 
e.l.f. Cosmetics, Inc

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e.l.f Whoa Glow Broad Spectrum SPF30 Sunscreen

Drug Facts

Active Ingredients

Avobenzone 3.0%

Homosalate 9.0%

Octisalate 5.0%

Octocrylene 7.0%

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 thsi 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.
• 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. Sun Protection Measures:

Other Information

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

Inactive Ingredients

Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Bismuth Oxychloride, Niacinamide, Aluminum Starch Octenylsuccinate, Trehalose, Silica, Panthenol, Sodium Hyaluronate, Squalane, Aloe Barbadensis Leaf Juice, Glyceryl Stearate Citrate, Cetearyl Olivate, Sorbitan Olivate, Stearyl Caprylate, Stearic Acid, Palmitic Acid, Dimethicone, Cetearyl Alcohol, Stearyl Heptanoate, Polyacrylate-13, Polyisobutene, Polysorbate 20, Ethylhexyl Hydroxystearate, Sorbitan Isostearate, Triethoxycaprylylsilane, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Caprylyl Glycol, Ethylhexylglycerin, Potassium Sorbate, Phenoxyethanol, Disodium EDTA, Sodium Benzoate, Citric Acid May Contain: Iron Oxides (CI 77491, CI 77492, CI 77499)

Questions or comments?

1-888-315-9814

Package Labeling:

Package Labeling:10ml

E.L.F WHOA GLOW BROAD SPECTRUM SPF30 SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-443
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	90 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
NIACINAMIDE (UNII: 25X51I8RD4)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
TREHALOSE (UNII: B8WCK70T7I)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PANTHENOL (UNII: WV9CM0O67Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SQUALANE (UNII: GW89575KF9)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
STEARYL CAPRYLATE (UNII: 06TS6O9194)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
DIMETHICONE (UNII: 92RU3N3Y1O)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-443-03	1 in 1 CARTON	09/15/2022
1		50 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 76354-443-02	1 in 1 CARTON	09/15/2022
2		10 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	09/15/2022	12/18/2024

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

Revised: 12/2024

Document Id: 298e8074-09f1-eb38-e063-6394a90ae4ef

34390-5

Set id: e452c7f3-d09b-15e0-e053-2a95a90afb10

Version: 5

Effective Time: 20241218