E L F CAMO SEMI MATTE CC SPF 30 LIGHT 205 N- zinc oxide, titanium dioxide, homosalate, octisalate, octocrylene cream

e l f Camo Semi Matte CC SPF 30 Light 205 N by

Drug Labeling and Warnings

e l f Camo Semi Matte CC SPF 30 Light 205 N 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

Zinc Oxide 6.3%

Titanium Dioxide 6%

Homosalate 5%

Octisalate 4.5%

Octocrylene 3%

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.

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 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), Dimethicone, Butylene Glycol, Silica, Cetyl PEG/PPG-10/1 Dimethicone, Isononyl Isononanoate, Butyloctyl Salicylate, Polyglyceryl-4 Isostearate, Magnesium Sulfate, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Trehalose, Phenoxyethanol, Hydrated Silica, Disteardimonium Hectorite, Triethoxycaprylylsilane, Hydrogen Dimethicone, Aluminum Hydroxide, Triethyl Citrate, Ethylhexylglycerin, Caprylyl Glycol, Disodium EDTA, Tocopheryl Acetate, Sodium Hyaluronate, Panthenol, Niacinamide, Ascorbyl Palmitate, Canola Oil, Glycerin, Daucus Carota Sativa (Carrot) Seed Oil, 1,2-Hexanediol, Carbomer, Daucus Carota Sativa (Carrot) Root Extract, Polysorbate 20, Helianthus Annuus (Sunflower) Seed Oil, Beta-Carotene, Soluble Collagen, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7 May Contain:Titanium Dioxide (CI 77891), Yellow Iron Oxide (CI 77492), Red Iron Oxide (CI 77491), Black Iron Oxide (CI 77499)

Questions or comments?

1-888-315-9814

Label

INGREDIENTS AND APPEARANCE

E L F CAMO SEMI MATTE CC SPF 30 LIGHT 205 N 
zinc oxide, titanium dioxide, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-532
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	63 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	60 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	50 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CARROT (UNII: L56Z1JK48B)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SUNFLOWER OIL (UNII: 3W1JG795YI)
BETA CAROTENE (UNII: 01YAE03M7J)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
TREHALOSE (UNII: B8WCK70T7I)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EDETATE DISODIUM (UNII: 7FLD91C86K)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PANTHENOL (UNII: WV9CM0O67Z)
NIACINAMIDE (UNII: 25X51I8RD4)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
CANOLA OIL (UNII: 331KBJ17RK)
GLYCERIN (UNII: PDC6A3C0OX)
CARROT SEED OIL (UNII: 595AO13F11)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-532-01	1 in 1 CARTON	02/15/2024
1		30 g 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	02/15/2024

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