CAMO CC SPF 30 DEEP 530 W- octinoxate, titanium dioxide, zinc oxide cream

Camo CC SPF 30 Deep 530 W by

Drug Labeling and Warnings

Camo CC SPF 30 Deep 530 W 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

Octinoxate 7.5% Titanium Dioxide 4.45% Zinc Oxide 13.72%

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 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
• Spending time in the sun increases your risk of sun 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 the sun, especially from 10 a.m.-2 p.m., wear long-sleeved shirt, 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), Dimethicone, Cyclopentasiloxane, Butylene Glycol, Phenyl Trimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Butylene Glycol Dicaprylate/Dicaprate, Butyloctyl Salicylate, Polyglyceryl-4 Isostearate, Methyl methacrylate Crosspolymer, Cyclohexasiloxane, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Hexyl Laurate, Magnesium Sulfate, Phenoxyethanol, Triethoxycaprylylsilane, Disteardimonium Hectorite, Hydrated Silica, Aluminum Hydroxide, Propylene Carbonate, Dimethicone/Methicone Copolymer, Caprylyl Glycol, Ethylhexylglycerin, Disodium EDTA, Tocopheryl Acetate, Sodium Hyaluronate, Niacinamide, Panthenol, Ascorbyl Palmitate, Soluble Collagen, Canola Oil, Glycerin, Daucus Carota Sativa (Carrot) Seed Oil, Carbomer, Daucus Carota Sativa (Carrot) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, Beta-Carotene, Polysorbate 20, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, 1,2-Hexanediol Titanium Dioxide (CI 77891), Yellow Iron Oxide (CI 77492), Red Iron Oxide (CI 77491), Black Iron Oxide (CI 77499) May Contain:

Questions or comments?

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Package Labeling:

INGREDIENTS AND APPEARANCE

CAMO CC SPF 30 DEEP 530 W 
octinoxate, titanium dioxide, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-869
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	44.5 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	137.2 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CARROT (UNII: L56Z1JK48B)
SUNFLOWER OIL (UNII: 3W1JG795YI)
BETA CAROTENE (UNII: 01YAE03M7J)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
NIACINAMIDE (UNII: 25X51I8RD4)
PANTHENOL (UNII: WV9CM0O67Z)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
CANOLA OIL (UNII: 331KBJ17RK)
GLYCERIN (UNII: PDC6A3C0OX)
CARROT SEED OIL (UNII: 595AO13F11)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-869-01	1 in 1 BOX	08/01/2021
1		30 g in 1 BOTTLE; 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	08/01/2021

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