Label: OLAY COMPLETE UV365 DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 30 SENSITIVE- octinoxate, octisalate, octocrylene, and zinc oxide lotion
- NDC Code(s): 69423-258-75
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 21, 2024
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
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Uses
- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
- 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
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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 sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months: ask a doctor
- Other information
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Inactive ingredients
Water, isohexadecane, glycerin, niacinamide, panthenol, camellia sinensis leaf extract, tocopheryl acetate, aloe barbadensis leaf extract, steareth-21, cyclopentasiloxane, polyacrylamide, stearyl alcohol, polymethylsilsesquioxane, polyethylene, C13-14 isoparaffin, behenyl alcohol, DMDM hydantoin, cetyl alcohol, triethoxycaprylylsilane, PEG/PPG-20/20 dimethicone, laureth-7, steareth-2, oleth-3 phosphate, disodium EDTA, iodopropynyl butylcarbamate.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OLAY COMPLETE UV365 DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 30 SENSITIVE
octinoxate, octisalate, octocrylene, and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-258 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2.5 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 7 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOHEXADECANE (UNII: 918X1OUF1E) GLYCERIN (UNII: PDC6A3C0OX) STEARETH-21 (UNII: 53J3F32P58) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ALOE VERA LEAF (UNII: ZY81Z83H0X) PANTHENOL (UNII: WV9CM0O67Z) NIACINAMIDE (UNII: 25X51I8RD4) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) DOCOSANOL (UNII: 9G1OE216XY) DMDM HYDANTOIN (UNII: BYR0546TOW) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETYL ALCOHOL (UNII: 936JST6JCN) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K) LAURETH-7 (UNII: Z95S6G8201) STEARETH-2 (UNII: V56DFE46J5) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) EDETATE DISODIUM (UNII: 7FLD91C86K) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-258-75 1 in 1 CARTON 06/21/2017 1 75 mL in 1 BOTTLE, PUMP; 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 06/21/2017 Labeler - The Procter & Gamble Manufacturing Company (004238200)
