NEUTROGENA INVISIBLE DAILY DEFENSE FACE SERUM SUNSCREEN BROAD SPECTRUM SPF 60- avobenzone, homosalate, octisalate, octocrylene lotion

Neutrogena Invisible Daily Defense Face Serum Sunscreen Broad Spectrum SPF 60 by

Drug Labeling and Warnings

Neutrogena Invisible Daily Defense Face Serum Sunscreen Broad Spectrum SPF 60 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 (13.5%),

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 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

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

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?

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

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Distributed by:

Kenvue Brands LLC

Summit, NJ 07901

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton Label

NEW FORMULA

Neutrogena ®

DERMATOLOGIST

RECOMMENDED BRAND

Invisible Daily

defense

face serum

Sunscreen

60

BROAD SPECTRUM SPF 60

DAILY HYDRATION

ANTIOXIDANTS + HUMECTANTS

all-day hydration

with HELIOPLEX ®

uva·uvb protection

sensitive skin

1.7 FL. OZ. (50 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA INVISIBLE DAILY DEFENSE FACE SERUM SUNSCREEN BROAD SPECTRUM SPF 60 
avobenzone, homosalate, octisalate, octocrylene lotion

Product 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)