Label: CAMO CC CREAM SPF30 RICH 660 N- octinoxate, titanium dioxide, zinc oxide cream
- NDC Code(s): 76354-929-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Use
- Warnings
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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 sun screen 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
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Inactive Ingredients
Water (Aqua), Dimethicone, Cylopentasiloxane, 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, Triethoxycaprylylylsilane, Disteardimonium Hectorite, Hydrated Silica, Aluminium Hydroxide, Propylene Carbonate, Dimethicone/Methicone Copolymer, Caprylyl Glycol, Ethylhexylglycerin, Disodium Edta, Tocopheryl Acetate, Sodium Hyaluronate, Niacinamide, Panthenol, Ascorbyl Palmitate, Soluble Collagen, Canola Oil, Glycerin, Daucu Carota Sativa (Carrot) See Oil, Carbomer, Daucus Carota Sativa (Carrot) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, Beta-Carotene, Poly-sorbate 20, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, 1,2-Hexanediol Titanium Dioxide (CI 77891), Yellow Iron Oxide(CI 77492), Red Iron Oxide (CI77491), Black Iron Oxide (CI 77499)
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INGREDIENTS AND APPEARANCE
CAMO CC CREAM SPF30 RICH 660 N
octinoxate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-929 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 WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) 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) 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) CARROT (UNII: L56Z1JK48B) SUNFLOWER OIL (UNII: 3W1JG795YI) BETA CAROTENE (UNII: 01YAE03M7J) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-929-01 1 in 1 BOX 09/01/2020 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 09/01/2020 Labeler - e.l.f. Cosmetics, Inc (093902816) Establishment Name Address ID/FEI Business Operations Zhejiang Ayan Biotech Co.,Ltd. 544377996 manufacture(76354-929)
