![OLAY SUN FACIAL SUNSCREEN ANTIOXIDANTS MAKEUP PRIMER SPF 35 (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) LOTION [THE PROCTER & GAMBLE MANUFACTURING COMPANY]](https://medic.hrt.org//dailymed/images/7f70ff87-50df-d54c-e053-2991aa0a32f9/Olay.jpg)
| NDC | 69423-335-40 |
| Set ID | 7f70ff87-50df-d54c-e053-2991aa0a32f9 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | The Procter & Gamble Manufacturing Company |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART352 |
- 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, tapioca starch, dimethicone, niacinamide*, tocopheryl acetate**, BHT, caprylyl glycol, dimethiconol, cetearyl glucoside, cetearyl alcohol, camellia sinensis leaf extract***, stearic acid, palmitic acid, disodium EDTA, PEG-100 stearate, polymethylsilsesquioxane, sodium polyacrylate starch, 1,2-hexanediol, phenoxyethanol, iodopropynyl butylcarbamate, fragrance
*Vitamin B3, **Vitamin E, ***Green Tea
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL 40mL Bottle Carton
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INGREDIENTS AND APPEARANCE
OLAY SUN FACIAL SUNSCREEN ANTIOXIDANTS MAKEUP PRIMER SPF 35
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-335 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 8.5 g in 100 mL Inactive Ingredients Ingredient Name Strength STARCH, TAPIOCA (UNII: 24SC3U704I) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) DIMETHICONE (UNII: 92RU3N3Y1O) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) EDETATE DISODIUM (UNII: 7FLD91C86K) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARIC ACID (UNII: 4ELV7Z65AP) PALMITIC ACID (UNII: 2V16EO95H1) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONOL GUM (UNII: 4MJ9GU3T1P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-335-40 1 in 1 CARTON 11/27/2018 05/26/2022 1 40 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 not final part352 11/27/2018 05/26/2022 Labeler - The Procter & Gamble Manufacturing Company (004238200)
