Label: RESTING BEACH FACE SPF30 ANTI-POLLUTION SUNSCREEN SERUM- butyl methoxydibenzoylmethane, homosalate, octyl salicylate, octocrylene cream
- NDC Code(s): 72098-001-01, 72098-001-03, 72098-001-05
- Packager: Everyday Group Limted
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
• Apply liberally 15 minutes before sun exposure • Use a water resistant sunscreen if swimming or sweating • Reapply at least every 2 hours • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the 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 to 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months of age: Ask a doctor
Sun Protection Measures: -
Inactive ingredients
Water (Aqua), Cyclomethicone, Isostearyl Neopentanoate, Glycerin, Ceteareth-20, Cetearyl Alcohol, Sodium Hyaluronate, Spinacia Oleracea Leaf Extract, Alteromonas Ferment Extract, Camellia Sinensis Leaf Extract, Caprylyl Glycol, Saccharide Isomerate, Xanthan Gum, PEG-40 Stearate, Triacontanyl PVP, Silica, Ammonium Acryloyldimethyltaurate/VP Copolymer, Butylene Glycol, Cetyl Dimethicone, Caprylhydroxamic Acid, Disodium EDTA, Parfum*, Tocopheryl Acetate, Helianthus Annuus Seed Oil, Triethanolamine, Citric Acid, Sodium Citrate, Potassium Sorbate *Natural Fragrance
- Other Information
- Package Labeling: 50 mL
- Package Labeling:5ml
- Package Labeling: 15ml
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INGREDIENTS AND APPEARANCE
RESTING BEACH FACE SPF30 ANTI-POLLUTION SUNSCREEN SERUM
butyl methoxydibenzoylmethane, homosalate, octyl salicylate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72098-001 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 HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q) GLYCERIN (UNII: PDC6A3C0OX) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ALTEROMONAS MACLEODII POLYSACCHARIDES (UNII: AP6XG2GR8Z) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SACCHARIDE ISOMERATE (UNII: W8K377W98I) XANTHAN GUM (UNII: TTV12P4NEE) PEG-40 STEARATE (UNII: ECU18C66Q7) TRICONTANYL POVIDONE (UNII: N0SS3Q238D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SUNFLOWER OIL (UNII: 3W1JG795YI) TROLAMINE (UNII: 9O3K93S3TK) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CITRATE (UNII: 1Q73Q2JULR) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72098-001-01 1 in 1 BOX 03/09/2020 1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:72098-001-05 5 mL in 1 TUBE; Type 0: Not a Combination Product 08/01/2020 3 NDC:72098-001-03 1 in 1 BOX 08/01/2021 3 15 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 03/09/2020 Labeler - Everyday Group Limted (664624682)
