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
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 July 28, 2023
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- 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) DOCOSANOL (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) MEDIUM-CHAIN TRIGLYCERIDES (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 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 final M020 03/01/2023 Labeler - The Procter & Gamble Manufacturing Company (004238200)