Drug Facts

Active ingredients	Purpose
Avobenzone 2.5%	Sunscreen
Homosalate 6%	Sunscreen
Octisalate 4.5%	Sunscreen
Octocrylene 8%	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, Silica, Caprylyl Methicone, Diisopropyl Adipate, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Beeswax, Glyceryl Stearate, PEG-100 Stearate, Cetyl Dimethicone, Caprylyl Glycol, Ethylhexylglycerin, Behenyl Alcohol, Sodium Polyacrylate, Acrylates/Dimethicone Crosspolymer, Xanthan Gum, Chlorphenesin, Dimethicone/PEG-10/15 Crosspolymer, Ethylhexyl Stearate, Hydrolyzed Jojoba Esters, Fragrance, Disodium EDTA, Tocopheryl Acetate, BHT, Trideceth-6, Jojoba Esters

Questions or Comments?

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

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

PRINCIPAL DISPLAY PANEL - 147 mL Tube Label

NEW LOOK / VALUE SIZE

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

ULTRA

SHEER ®

Dry-Touch

Sunscreen

BROAD SPECTRUM SPF 30

Antioxidant Vitamin E

Lightweight clean feel

Shields skin 6 layers deep

with helioplex ®

Water resistant (80 minutes)

5.0 FL OZ (147 mL)

Neutrogena_01

NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF 30
avobenzone, homosalate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0552
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	25 mg in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	60 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DOCOSANOL (UNII: 9G1OE216XY)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
XANTHAN GUM (UNII: TTV12P4NEE)
CHLORPHENESIN (UNII: I670DAL4SZ)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
DIMETHICONE (UNII: 92RU3N3Y1O)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
YELLOW WAX (UNII: 2ZA36H0S2V)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69968-0552-5	147 mL in 1 TUBE; Type 0: Not a Combination Product	10/07/2019
2	NDC:69968-0552-3	88 mL in 1 TUBE; Type 0: Not a Combination Product	10/07/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	10/07/2019

Labeler - Johnson & Johnson Consumer Inc. (118772437)