Label: NEUTROGENA INVISIBLE DAILY DEFENSE BROAD SPECTRUM SPF 30- avobenzone, homosalate, octisalate, and octocrylene lotion
- NDC Code(s): 69968-0842-3
- 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
- Uses
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
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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, Glycerin, Diisopropyl Adipate, Dimethicone, Alcohol Denat., Silica, Dicaprylyl Carbonate, Caprylyl Methicone, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Polyurethane-62, Pentylene Glycol, Hydroxyacetophenone, Acrylates/Dimethicone Copolymer, Glyceryl Stearate, Phenoxyethanol, Chlorphenesin, Dimethicone Crosspolymer, Fragrance, Tocopheryl Acetate, Disodium EDTA, Sodium Hydroxide, Trideceth-6, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Yellow 5, Red 40
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 88 mL Tube Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA INVISIBLE DAILY DEFENSE BROAD SPECTRUM SPF 30
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0842 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 15 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 60 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) DIMETHICONE (UNII: 92RU3N3Y1O) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) PENTYLENE GLYCOL (UNII: 50C1307PZG) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM HYDROXIDE (UNII: 55X04QC32I) TRIDECETH-6 (UNII: 3T5PCR2H0C) FEVERFEW (UNII: Z64FK7P217) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 40 (UNII: WZB9127XOA) POLYURETHANE-62 (UNII: TBK645J3J8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0842-3 88 mL in 1 TUBE; Type 0: Not a Combination Product 01/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/31/2024 Labeler - Kenvue Brands LLC (118772437)