Label: SEPHORA 8HR MATTIFYING MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 20- avobenzone, octinoxate, octocrylene cream
- NDC Code(s): 31720-202-10
- Packager: S+
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
for sunscreen use
- Apply liberally 15 minutes before sun exposure
- Reapply at least every 2 hours
- Use a water resistant sunscreen if swimming or sweating
- Sun Protection Measures. 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 the 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
- Other Information
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Inactive Ingredients
WATER, DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, GLYCERIN, POLYSORBATE 20, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, DIMETHICONE CROSSPOLYMER, SORBITOL, SQUALANE, BUTYLENE GLYCOL, PANTHENOL, POLYSORBATE 60, POMEGRANATE (PUMICA GRANATUM) EXTRACT, TOCOPHERYL ACETATE, SENNA (CASSIA ANGUSTIFOLIA) SEED POLYSACCHARIDE, ENANTIA CHLORANTHA BARK EXTRACT, OLEANOLIC ACID, CAPRYLYL GLYCOL, PHENOXYETHANOL, FRAGRANCE
- Pakage Labeling:
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INGREDIENTS AND APPEARANCE
SEPHORA 8HR MATTIFYING MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 20
avobenzone, octinoxate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:31720-202 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 OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 23.7 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITOL (UNII: 506T60A25R) SQUALANE (UNII: GW89575KF9) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PANTHENOL (UNII: WV9CM0O67Z) POLYSORBATE 60 (UNII: CAL22UVI4M) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A) OLEANOLIC ACID (UNII: 6SMK8R7TGJ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:31720-202-10 1 in 1 CARTON 11/19/2012 1 50 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 11/19/2012 Labeler - S+ (572406531)
