Label: NEUTROGENA MINERAL ULTRA SHEER FACE SPF 70- titanium dioxide, zinc oxide lotion
- NDC Code(s): 69968-0895-1, 69968-0895-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 12, 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
For Sunscreen Use:
- apply generously 15 minutes before sun exposure
- reapply at least every 2 hours
- use a 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 the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
Water, Caprylic/Capric Triglyceride, Glycerin, Butyloctyl Salicylate, Ethylhexyl Methoxycrylene, VP/Hexadecene Copolymer, Dimethicone, Steareth-21, Calcium Sodium Borosilicate, Triacontanyl PVP, Polyhydroxystearic Acid, Aluminum Hydroxide, Stearic Acid, Triethoxycaprylylsilane, Cetearyl Olivate, Phenoxyethanol, Sodium Chloride, Xanthan Gum, Ethylhexylglycerin, Sorbitan Olivate, Chlorphenesin, Caprylyl Glycol, Tocopheryl Acetate, Disodium EDTA
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 40 mL Carton Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA MINERAL ULTRA SHEER FACE SPF 70
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0895 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 144 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 66 mg in 1 mL Inactive Ingredients Ingredient Name Strength XANTHAN GUM (UNII: TTV12P4NEE) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9) DIMETHICONE (UNII: 92RU3N3Y1O) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CETEARYL OLIVATE (UNII: 58B69Q84JO) CHLORPHENESIN (UNII: I670DAL4SZ) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM CHLORIDE (UNII: 451W47IQ8X) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) TRICONTANYL POVIDONE (UNII: N0SS3Q238D) CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY) SORBITAN OLIVATE (UNII: MDL271E3GR) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE DISODIUM (UNII: 7FLD91C86K) STEARETH-21 (UNII: 53J3F32P58) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0895-1 1 in 1 CARTON 09/06/2024 1 40 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69968-0895-2 24 in 1 TRAY 09/06/2024 2 1.4 mL in 1 POUCH; 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 09/06/2024 Labeler - Kenvue Brands LLC (118772437)
