Label: OLAY REGENERIST WHIP ACTIVE MOISTURIZER BROAD SPECTRUM SPF 40 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone cream
- NDC Code(s): 69423-359-48
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 January 12, 2023
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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, tapioca starch, glycerin, niacinamide, dimethicone, palmitoyl pentapeptide-4, sodium hyaluronate, panthenol, sodium polyacrylate starch, stearyl alcohol, caprylyl glycol, behenyl alcohol, 1,2-hexanediol, phenoxyethanol, cetyl alcohol, dimethiconol, PEG-100 stearate, fragrance, polymethylsilsesquioxane, ceratonia siliqua (carob) fruit extract, cetearyl glucoside, cetearyl alcohol, disodium EDTA, stearic acid, palmitic acid.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 48 g Jar Carton
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INGREDIENTS AND APPEARANCE
OLAY REGENERIST WHIP ACTIVE MOISTURIZER BROAD SPECTRUM SPF 40 SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-359 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9 g in 100 g Inactive Ingredients Ingredient Name Strength CAROB (UNII: 5MG5Z946UO) STARCH, TAPIOCA (UNII: 24SC3U704I) HYALURONATE SODIUM (UNII: YSE9PPT4TH) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) NIACINAMIDE (UNII: 25X51I8RD4) PANTHENOL (UNII: WV9CM0O67Z) PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) PEG-100 STEARATE (UNII: YD01N1999R) DOCOSANOL (UNII: 9G1OE216XY) CETYL ALCOHOL (UNII: 936JST6JCN) EDETATE DISODIUM (UNII: 7FLD91C86K) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARIC ACID (UNII: 4ELV7Z65AP) PALMITIC ACID (UNII: 2V16EO95H1) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) DIMETHICONOL GUM (UNII: 4MJ9GU3T1P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-359-48 1 in 1 CARTON 09/01/2019 1 48 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 not final part352 09/01/2019 Labeler - The Procter & Gamble Manufacturing Company (004238200)
