Label: NEUTROGENA INVISIBLE DAILY DEFENSE FACE SERUM SUNSCREEN BROAD SPECTRUM SPF 60- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 69968-0961-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 15, 2026
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Uses
- Warnings
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Directions
For Sunscreen Use:
● apply liberally 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, Butyloctyl Salicylate, Glycerin, Silica, Triacontanyl PVP, Trilaureth-4 Phosphate, Aluminum Starch Octenylsuccinate, Dimethicone, Phenoxyethanol, Hydroxyacetophenone, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Glyceryl Stearate, Chlorphenesin, Disodium EDTA, Tocopheryl Acetate, Zingiber Officinale (Ginger) Root Extract, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Sodium Hydroxide, Yellow 5, Red 40
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA INVISIBLE DAILY DEFENSE FACE SERUM SUNSCREEN BROAD SPECTRUM SPF 60
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0961 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 135 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) GLYCERIN (UNII: PDC6A3C0OX) EDETATE DISODIUM (UNII: 7FLD91C86K) TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) CHLORPHENESIN (UNII: I670DAL4SZ) GINGER (UNII: C5529G5JPQ) SILICA (UNII: ETJ7Z6XBU4) FEVERFEW (UNII: Z64FK7P217) SODIUM HYDROXIDE (UNII: 55X04QC32I) YELLOW 5 (UNII: I753WB2F1M) RED 40 (UNII: WZB9127XOA) WATER (UNII: 059QF0KO0R) TRIACONTANYL PVP (UNII: N0SS3Q238D) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL STEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0961-2 1 in 1 CARTON 04/01/2026 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 Drug M020 04/01/2026 Labeler - Kenvue Brands LLC (118772437)
