| NDC | 69423-207-50 |
| Set ID | 54102354-d9eb-0491-e054-00144ff8d46c |
| 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
-
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
-
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
-
Inactive ingredients
water, glycerin, polymethylsilsesquioxane, niacinamide*, polyethylene, pentylene glycol, palmitoyl pentapeptide-4**, panthenol***, tocopheryl acetate^, camellia sinensis leaf extract^^, allantoin, carnosine, dimethicone, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, benzyl alcohol, titanium dioxide, stearyl alcohol, behenyl alcohol, polyacrylamide, PEG-100 stearate, cetyl alcohol, methylparaben, propylparaben, fragrance, ethylparaben, C13-14 isoparaffin, cetearyl glucoside, cetearyl alcohol, dimethiconol, sodium ascorbyl phosphate, citric acid, BHT, laureth-7, disodium EDTA, stearic acid, palmitic acid, iodopropynyl butylcarbamate.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
OLAY LUMINOUS BRIGHTENING AND PROTECTING WITH SUNSCREEN BROAD SPECTRUM SPF 30
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-207 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 15 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2.6 g in 100 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 6 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) NIACINAMIDE (UNII: 25X51I8RD4) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) PENTYLENE GLYCOL (UNII: 50C1307PZG) DIMETHICONE (UNII: 92RU3N3Y1O) PANTHENOL (UNII: WV9CM0O67Z) PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG) CARNOSINE (UNII: 8HO6PVN24W) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ALLANTOIN (UNII: 344S277G0Z) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) PEG-100 STEARATE (UNII: YD01N1999R) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) DOCOSANOL (UNII: 9G1OE216XY) CETYL ALCOHOL (UNII: 936JST6JCN) EDETATE DISODIUM (UNII: 7FLD91C86K) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) BENZYL ALCOHOL (UNII: LKG8494WBH) STEARIC ACID (UNII: 4ELV7Z65AP) ETHYLPARABEN (UNII: 14255EXE39) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) LAURETH-7 (UNII: Z95S6G8201) PALMITIC ACID (UNII: 2V16EO95H1) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-207-50 1 in 1 CARTON 04/24/2017 12/04/2021 1 50 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 not final part352 04/24/2017 12/04/2021 Labeler - The Procter & Gamble Manufacturing Company (004238200)
