Label: OLAY SENSITIVE MINERAL SUNSCREEN WITH COLLOIDAL OATMEAL BROAD SPECTRUM SPF 30- zinc oxide lotion
- NDC Code(s): 69423-723-50
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 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, caprylic/capric triglyceride, isohexadecane, glycerin, steareth-21, polyhydroxystearic acid, colloidal oatmeal, niacinamide*, palmitoyl pentapeptide-4**, hydroxyacetophenone, C13-14 isoparaffin, steareth-2, laureth-7, stearyl alcohol, behenyl alcohol, cetyl alcohol, disodium EDTA, polyacrylamide, triethoxycaprylylsilane, phenoxyethanol
- SPL UNCLASSIFIED SECTION
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- PRINCIPAL DISPLAY PANEL - 50 mL Carton
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INGREDIENTS AND APPEARANCE
OLAY SENSITIVE MINERAL SUNSCREEN WITH COLLOIDAL OATMEAL BROAD SPECTRUM SPF 30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-723 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 17.5 g in 100 mL Inactive Ingredients Ingredient Name Strength OATMEAL (UNII: 8PI54V663Y) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) STEARETH-21 (UNII: 53J3F32P58) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) BEHENYL ALCOHOL (UNII: 9G1OE216XY) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CETYL ALCOHOL (UNII: 936JST6JCN) STEARETH-2 (UNII: V56DFE46J5) EDETATE DISODIUM (UNII: 7FLD91C86K) LAURETH-7 (UNII: Z95S6G8201) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) NIACINAMIDE (UNII: 25X51I8RD4) POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG) PHENOXYETHANOL (UNII: HIE492ZZ3T) PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-723-50 1 in 1 CARTON 03/01/2023 08/01/2025 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 Drug M020 03/01/2023 08/01/2025 Labeler - The Procter & Gamble Manufacturing Company (004238200)
