- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
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Uses
- Helps prevent sunburn.
- If used as directed with other sun protection measures (see Directions), helps decrease the risk of skin cancer and early skin aging caused by the sun.
- Warnings
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Directions
- Apply liberally 30 minutes before sun exposure
- Reapply at least every two hours
- Use a water-resistant sunscreen if swimming or sweating
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Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To help decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 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-sleeve shirts, pants, hats and sunglasses
- Do not use on infants under 6 months old.
- Other information
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Inactive ingredients
Water/Aqua/Eau, Carthamus Tinctorius (Safflower) Oleosomes, Butylene Glycol, Glycerin, C12-15 Alkyl Benzoate, Polysorbate 80, Dimethyl Capramide, Sodium Hyaluronate Crosspolymer, Cananga Odorata Flower Oil, Eucalyptus Globulus Leaf Oil, Lavandula Hybrida Oil, Lavendula Spica (Lavender) Flower Oil, Laminaria Ochroleuca Extract, Palmaria Palmata Extract, Oligopeptide-34, Dipotassium Glycyrrhizate, Lactobacillus/Pumpkin Fruit Ferment Filtrate, Niacinamide, Zinc Glycinate, Polysorbate 60, Ammonium Acryloyldimethyltaurate/VP Copolymer, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Butylene Glycol Behenate, Glyceryl Polyacrylate, Disodium EDTA, Sodium Hydroxide, Ethylhexylglycerin, Phenoxyethanol.
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton
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INGREDIENTS AND APPEARANCE
PURELIGHT SPF50
avobenzone and octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68479-213 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 Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 75 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Carthamus Tinctorius Seed Oleosomes (UNII: 9S60Q72309) Butylene Glycol (UNII: 3XUS85K0RA) Glycerin (UNII: PDC6A3C0OX) Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ) Polysorbate 80 (UNII: 6OZP39ZG8H) Dimethyl Capramide (UNII: O29Y6X2JEZ) Cananga Oil (UNII: 8YOY78GNNX) Eucalyptus Oil (UNII: 2R04ONI662) Lavandin Oil (UNII: 9RES347CKG) Lavender Oil (UNII: ZBP1YXW0H8) Laminaria Ochroleuca (UNII: 4R2124HE76) Dulse (UNII: 7832HOY4ZQ) Glycyrrhizinate Dipotassium (UNII: CA2Y0FE3FX) Niacinamide (UNII: 25X51I8RD4) Zinc Glycinate (UNII: 681VJX72FE) Polysorbate 60 (UNII: CAL22UVI4M) Ammonium Acryloyldimethyltaurate/VP Copolymer (UNII: W59H9296ZG) Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer (100000 MPA.S at 1.5%) (UNII: 86FQE96TZ4) Isohexadecane (UNII: 918X1OUF1E) Butylene Glycol Behenate (UNII: X0IW5BP6ZL) Edetate Disodium (UNII: 7FLD91C86K) Sodium Hydroxide (UNII: 55X04QC32I) Ethylhexylglycerin (UNII: 147D247K3P) Phenoxyethanol (UNII: HIE492ZZ3T) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68479-213-02 1 in 1 CARTON 02/18/2014 1 50 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:68479-213-00 2 mL in 1 POUCH; Type 0: Not a Combination Product 02/18/2014 3 NDC:68479-213-01 10 mL in 1 TUBE; Type 0: Not a Combination Product 02/18/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part352 02/18/2014 Labeler - Dermalogica, Inc. (177698560) Establishment Name Address ID/FEI Business Operations THIBIANT 083913913 MANUFACTURE(68479-213) Establishment Name Address ID/FEI Business Operations Diamond Wipes 161104729 MANUFACTURE(68479-213)