Label: NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide, zinc oxide lotion
- NDC Code(s): 69968-0815-1, 69968-0815-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
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Directions
Shake bottle well before use.
• For Sunscreen Use:
• apply generously 15 minutes before sun exposure
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• 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, Zingiber Officinale (Ginger) Root Extract, Tocopheryl Acetate, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Calcium Sodium Borosilicate, Polyhydroxystearic Acid, Triethoxycaprylylsilane, Sorbitan Sesquioleate, Sodium Chloride, Aluminum Hydroxide, Phenoxyethanol, Triacontanyl PVP, Ethylhexylglycerin, Stearic Acid, Iron Oxides
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 40 mL Bottle Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0815 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 49 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 mL Inactive Ingredients Ingredient Name Strength SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GINGER (UNII: C5529G5JPQ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) STEARIC ACID (UNII: 4ELV7Z65AP) FERROUS OXIDE (UNII: G7036X8B5H) FEVERFEW (UNII: Z64FK7P217) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DICAPRYLYL ETHER (UNII: 77JZM5516Z) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0815-1 1 in 1 CARTON 08/21/2023 1 40 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69968-0815-2 24 in 1 TRAY 01/01/2024 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 08/21/2023 Labeler - Kenvue Brands LLC (118772437)
