Label: OLAY COMPLETE UV365 DAILY MOISTURIZER SENSITIVE BROAD SPECTRUM SPF 15- octinoxate and zinc oxide lotion
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NDC Code(s):
69423-194-01,
69423-194-02,
69423-194-12,
69423-194-17, view more69423-194-50
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 6, 2024
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- Official Label (Printer Friendly)
- 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, glycerin, isohexadecane, aloe barbadensis leaf extract, tocopheryl acetate, steareth-21, cyclopentasiloxane, polyacrylamide, stearyl alcohol, C13-14 isoparaffin, behenyl alcohol, DMDM hydantoin, cetyl alcohol, PEG/PPG-20/20 dimethicone, laureth-7, steareth-2, disodium EDTA, triethoxycaprylylsilane, oleth-3 phosphate, BHT, iodopropynyl butylcarbamate.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 177 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
OLAY COMPLETE UV365 DAILY MOISTURIZER SENSITIVE BROAD SPECTRUM SPF 15
octinoxate and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-194 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3 g in 100 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) STEARETH-21 (UNII: 53J3F32P58) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DOCOSANOL (UNII: 9G1OE216XY) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) DMDM HYDANTOIN (UNII: BYR0546TOW) CETYL ALCOHOL (UNII: 936JST6JCN) PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K) STEARETH-2 (UNII: V56DFE46J5) EDETATE DISODIUM (UNII: 7FLD91C86K) LAURETH-7 (UNII: Z95S6G8201) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-194-12 1 in 1 CARTON 09/11/2017 1 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:69423-194-17 1 in 1 CARTON 09/11/2017 2 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:69423-194-50 1 in 1 CARTON 09/11/2017 3 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:69423-194-01 0.5 mL in 1 POUCH; Type 0: Not a Combination Product 09/11/2017 5 NDC:69423-194-02 2 in 1 BLISTER PACK 02/03/2020 5 1 in 1 CARTON 5 177 mL in 1 BOTTLE, PLASTIC; 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 09/11/2017 Labeler - The Procter & Gamble Manufacturing Company (004238200) Establishment Name Address ID/FEI Business Operations The Procter & Gamble Manufacturing Company 017745779 manufacture(69423-194) , pack(69423-194)
