Label: OLAY COMPLETE ALL DAY MOISTURE SENSITIVE WITH BROAD SPECTRUM SPF 15- octinoxate and zinc oxide cream
- NDC Code(s): 37000-275-56
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 13, 2022
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- Official Label (Printer Friendly)
- 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), 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, isopropyl palmitate, isohexadecane, tocopheryl acetate, aloe barbadensis leaf extract, steareth-21, stearyl alcohol, cetyl alcohol, behenyl alcohol, dimethicone, polyacrylamide, C13-14 isoparaffin, DMDM hydantoin, steareth-2, disodium EDTA, dimethiconol, laureth-7, triethoxycaprylylsilane, oleth-3 phosphate, iodopropynyl butylcarbamate.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 56 g Jar Carton
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INGREDIENTS AND APPEARANCE
OLAY COMPLETE ALL DAY MOISTURE SENSITIVE WITH BROAD SPECTRUM SPF 15
octinoxate and zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-275 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) STEARETH-21 (UNII: 53J3F32P58) DOCOSANOL (UNII: 9G1OE216XY) CETYL ALCOHOL (UNII: 936JST6JCN) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DIMETHICONE (UNII: 92RU3N3Y1O) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) DMDM HYDANTOIN (UNII: BYR0546TOW) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) EDETATE DISODIUM (UNII: 7FLD91C86K) STEARETH-2 (UNII: V56DFE46J5) ALOE VERA LEAF (UNII: ZY81Z83H0X) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) POLYQUATERNIUM-5 (UNII: Q44R132386) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-275-56 1 in 1 CARTON 04/01/2012 06/30/2024 1 56 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 04/01/2012 06/30/2024 Labeler - The Procter & Gamble Manufacturing Company (004238200)
