Label: E.L.F INVISIBLE SUNSCREEN SPF 35- avobenzone, octisalate, octocrylene, homosalate cream
- NDC Code(s): 76354-444-01, 76354-444-02
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 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.
- After 80 minutes of swimming.
- Immediately after towel drying.
- At least every 2 hours.
- 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
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Inactive Ingredients
Isododecane, Dimethicone, Silica, Dimethyl Silylate, Caprylyl Methicone, PEG-10 Dimethicone/Vinyl Dimethicone Crosspolymer, Glycerin, PEG-12 Dimethicone/PPG-20 Crosspolymer, Pongamia Pinnata Seed Extract, Limnanthes Alba (Meadowfoam) Seed Oil, Aloe Barbadensis Leaf Juice Powder, Polyester-7, Neopentyl Glycol Diheptanoate, Phenoxyethanol, Ethylhexylglycerin, Isopropyl Palmitate
- Question or comments?
- Package Labeling:50ml
- Package Labeling:10ml
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INGREDIENTS AND APPEARANCE
E.L.F INVISIBLE SUNSCREEN SPF 35
avobenzone, octisalate, octocrylene, homosalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-444 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength ISODODECANE (UNII: A8289P68Y2) DIMETHICONE (UNII: 92RU3N3Y1O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) GLYCERIN (UNII: PDC6A3C0OX) PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO) PONGAMIA PINNATA SEED (UNII: C2BRV53B1V) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLYESTER-7 (UNII: 0841698D2F) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-444-01 1 in 1 CARTON 02/15/2023 1 50 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:76354-444-02 1 in 1 CARTON 02/15/2023 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 02/15/2023 Labeler - e.l.f. Cosmetics, Inc (093902816)