WHOA GLOW BROAD SPECTRUM SPF 30 SUNSCREEN SHEER CHAMPAGNE SHIMMER SUNLIGHT- avobenzone, homosalate, octisalate, octocrylene cream

Whoa Glow broad spectrum spf 30 sunscreen Sheer Champagne shimmer sunlight by

Drug Labeling and Warnings

Whoa Glow broad spectrum spf 30 sunscreen Sheer Champagne shimmer sunlight 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 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, Calcium Aluminum Borosilicate, Polyglyceryl-3 Distearate, Niacinamide, Trehalose, Silica, Aluminum Starch Octenylsuccinate, Stearyl Heptanoate, Aloe Barbadensis Leaf Juice, Panthenol, Squalane, Sodium Hyaluronate, Dimethicone, Cetearyl Alcohol, Synthetic Fluorphlogopite, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Palmitic Acid, Cetearyl Olivate, Stearic Acid, Sorbitan Olivate, Ethylhexylglycerin, Polyacrylate-13, Caprylyl Glycol, Polyisobutene, Polysorbate 20, Sorbitan Isostearate, Glyceryl Stearate Citrate, Phenoxyethanol, Disodium EDTA, Tin Oxide, Triethoxycaprylylsilane, Citric Acid, Potassium Sorbate, Sodium Benzoate May Contain: Titanium Oxide (CI 77891), Iron Oxide (CI 77492, CI 77491, CI 77499)

Questions or comments?

1-888-315-9814

Package Labeling:

INGREDIENTS AND APPEARANCE

WHOA GLOW BROAD SPECTRUM SPF 30 SUNSCREEN SHEER CHAMPAGNE SHIMMER SUNLIGHT 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-446
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)
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
NIACINAMIDE (UNII: 25X51I8RD4)
TREHALOSE (UNII: B8WCK70T7I)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PANTHENOL (UNII: WV9CM0O67Z)
SQUALANE (UNII: GW89575KF9)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
DIMETHICONE (UNII: 92RU3N3Y1O)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PALMITIC ACID (UNII: 2V16EO95H1)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN OLIVATE (UNII: MDL271E3GR)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYACRYLATE-13 (UNII: FS2D4T67EA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
STANNIC OXIDE (UNII: KM7N50LOS6)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-446-01	1 in 1 CARTON	05/15/2023
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	05/15/2023

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