Label: NEUTROGENA HYDRO BOOST HYALURONIC ACID MOISTURIZER BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, and octocrylene lotion
- NDC Code(s): 69968-0932-1, 69968-0932-2, 69968-0932-3
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 28, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
-
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
-
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
-
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
-
Inactive ingredients
Water, Butyloctyl Salicylate, Glycerin, Silica, Trilaureth-4 Phosphate, Triacontanyl PVP, Caprylic/Capric Triglyceride, Aluminum Starch Octenylsuccinate, Phenoxyethanol, Hydroxyacetophenone, Sodium Acryloyldimethyltaurate/VP Crosspolymer,
Dimethicone, Glyceryl Stearate, Chlorphenesin, Tocopheryl Acetate, Disodium EDTA, Ascorbic Acid, Hydrolyzed Hyaluronic Acid, Hydroxymethoxyphenyl Decanone, Sodium Hydroxide
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
NEUTROGENA HYDRO BOOST HYALURONIC ACID MOISTURIZER BROAD SPECTRUM SPF 50
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0932 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 135 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCERYL STEARATE (UNII: 230OU9XXE4) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) TRIACONTANYL PVP (UNII: N0SS3Q238D) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SILICA (UNII: ETJ7Z6XBU4) TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) HYDROXYMETHOXYPHENYL DECANONE (UNII: BO24ID7E9U) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ASCORBIC ACID (UNII: PQ6CK8PD0R) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0932-1 1 in 1 CARTON 09/01/2025 1 14 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:69968-0932-2 1 in 1 CARTON 09/01/2025 2 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 3 NDC:69968-0932-3 12 in 1 TRAY 09/01/2025 3 14 mL in 1 TUBE; 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 09/01/2025 Labeler - Kenvue Brands LLC (118772437)

