NEUTROGENA CLEAR FACE SERUM SUNSCREEN BROAD SPECTRUM SPF 60- avobenzone, homosalate, octisalate, octocrylene liquid

Neutrogena Clear Face Serum Sunscreen Broad Spectrum SPF 60 by

Drug Labeling and Warnings

Neutrogena Clear 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]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredients	Purpose
Avobenzone (3%)	Sunscreen
Homosalate (13.5%)	Sunscreen
Octisalate (5%)	Sunscreen
Octocrylene (10%)	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

▪ apply liberally 15 minutes before sun exposure

▪ reapply:

▪ after 80 minutes of swimming or sweating

▪ immediately after towel drying

▪ at least every 2 hours

▪ 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, Alcohol Denat., Silica, Dimethicone, Camellia Sinensis Leaf Extract, Aluminum Starch Octenylsuccinate, Polyurethane-62, Phenoxyethanol, Pentylene Glycol, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Bisabolol, Acrylates/Dimethicone Copolymer, Glyceryl Stearate, Chlorphenesin, Styrene/Acrylates Copolymer, Menthyl Lactate, Tocopheryl

Acetate, Disodium EDTA, Trideceth-6, Butylene Glycol, Sodium Hydroxide

Questions?

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

SPL UNCLASSIFIED SECTION

Distributed by: JOHNSON & JOHNSON CONSUMER INC. Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 50 mL Carton Label

Neutrogena ®

DERMATOLOGIST

RECOMMENDED BRAND

Clear Face

face serum

Sunscreen

60

BROAD SPECTRUM SPF 60

DAILY CLEAR SKIN

ANTIOXIDANT GREEN TEA

non-greasy protection.

won’t clog pores.

with HELIOPLEX ®

uva∙uvb protection

sensitive and acne prone skin

WATER RESISTANT (80 MINUTES)

1.7 FL OZ (50 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA CLEAR FACE SERUM SUNSCREEN BROAD SPECTRUM SPF 60 
avobenzone, homosalate, octisalate, octocrylene liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0828
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
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	135 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
LEVOMENOL (UNII: 24WE03BX2T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
POLYURETHANE-62 (UNII: TBK645J3J8)
CHLORPHENESIN (UNII: I670DAL4SZ)
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
ALCOHOL (UNII: 3K9958V90M)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0828-2	1 in 1 CARTON	01/01/2024
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	01/01/2024

Labeler - Kenvue Brands LLC (118772437)