NEUTROGENA ULTRA SHEER DRY-TOUCH SUNSCREEN MAX BROAD SPECTRUM SPF 100 PLUS- avobenzone, homosalate, octisalate, octocrylene lotion

Neutrogena Ultra Sheer Dry-Touch Sunscreen MAX Broad Spectrum SPF 100 Plus by

Drug Labeling and Warnings

Neutrogena Ultra Sheer Dry-Touch Sunscreen MAX Broad Spectrum SPF 100 Plus by is a Otc medication manufactured, distributed, or labeled by Kenvue Brands LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active ingredients

Avobenzone (3%), Homosalate (15%),

Octisalate (5%), Octocrylene (10%)

PURPOSE

Purpose

Sunscreen

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

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

● Stop use and ask a doctor if ● rash occurs.

● Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For Sunscreen Use:

● apply generously 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

• protect this product from excessive heat and direct sun
• may stain some fabrics
• protect from freezing

Inactive ingredients

Water, Ethylhexyl Methoxycrylene, Styrene/Acrylates Copolymer, Copernicia Cerifera (Carnauba) Wax, Hydrogenated Castor Oil, Silica, Triacontanyl PVP, Potassium Cetyl Phosphate, Caprylyl Methicone, Aluminum Starch Octenylsuccinate, Glyceryl Stearate, PEG-100 Stearate, Cetyl Dimethicone, Dimethicone, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Acrylates/Dimethicone Copolymer, Xanthan Gum, Chlorphenesin, Sodium Polyacrylate, Hydrolyzed Jojoba Esters, Disodium EDTA, Ethylhexyl Stearate, Tocopheryl Acetate, Jojoba Esters, Trideceth-6, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice

Questions?

Call toll-free 800-299-4786 or 215-273-8755 (collect). www.neutrogena.com

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Distributed by:

Kenvue Brands LLC

Summit, NJ 07901

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

ULTRA

SHEER®

Dry-Touch

Sunscreen

max

100+

BROAD SPECTRUM SPF 100+

With Antioxidants

Lightweight clean feel

Blocks up to 99% of UVB rays

with HELIOPLEX360 TM

3.0 FL OZ (88 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA ULTRA SHEER DRY-TOUCH SUNSCREEN MAX BROAD SPECTRUM SPF 100 PLUS 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0936
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	150 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
WATER (UNII: 059QF0KO0R)
TRIACONTANYL PVP (UNII: N0SS3Q238D)
DIMETHICONE (UNII: 92RU3N3Y1O)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
XANTHAN GUM (UNII: TTV12P4NEE)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
CHLORPHENESIN (UNII: I670DAL4SZ)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
SILICA (UNII: ETJ7Z6XBU4)
HYDROLYZED JOJOBA ESTERS (UNII: UDR641JW8W)
COPERNICIA CERIFERA (CARNAUBA) WAX (UNII: R12CBM0EIZ)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0936-3	88 mL in 1 TUBE; Type 0: Not a Combination Product	08/18/2025
2	NDC: 69968-0936-1	12 in 1 TRAY	08/18/2025
2		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	08/18/2025

Labeler - Kenvue Brands LLC (118772437)