Label: NEUTROGENA HEALTHY SKIN INVISIBLY RADIANT UV PRIMER SPF 30- titanium dioxide, zinc oxide lotion
- NDC Code(s): 69968-0900-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
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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 and evenly 15 minutes before sun exposure
- reapply at least every 2 hours
- use a 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 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, Isononyl Isononanoate,Dicaprylyl Ether, C12-15 Alkyl Benzoate, Polyglyceryl-2 Dipolyhydroxystearate, Propylene Glycol, Dimethicone, Calcium Sodium Borosilicate, Polyhydroxystearic Acid,Triethoxycaprylylsilane, Sorbitan Sesquioleate, Sodium Chloride, Aluminum Hydroxide, Triacontanyl PVP, Phenoxyethanol, Ethylhexylglycerin, Stearic Acid, Zingiber Officinale (Ginger) Root Extract, Tocopheryl Acetate, Mica, Titanium Dioxide, Iron Oxides
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 29 mL Tube Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA HEALTHY SKIN INVISIBLY RADIANT UV PRIMER SPF 30
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 49 mg in 1 mL Inactive Ingredients Ingredient Name Strength DICAPRYLYL ETHER (UNII: 77JZM5516Z) FERROUS OXIDE (UNII: G7036X8B5H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) STEARIC ACID (UNII: 4ELV7Z65AP) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIMETHICONE (UNII: 92RU3N3Y1O) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) PHENOXYETHANOL (UNII: HIE492ZZ3T) GINGER (UNII: C5529G5JPQ) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) TRICONTANYL POVIDONE (UNII: N0SS3Q238D) MICA (UNII: V8A1AW0880) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0900-1 29 mL in 1 TUBE; Type 0: Not a Combination Product 11/08/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/08/2024 Labeler - Kenvue Brands LLC (118772437)