Drug Facts

Active ingredients	Purpose
Titanium Dioxide (6.6%), Zinc Oxide (18.0%)	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, Isohexadecane, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Dimethicone, Ethylhexyl methoxycrylene, Caprylyl Methicone, Glyceryl Stearate, PEG-100 Stearate, Calcium Sodium Borosilicate, VP/Hexadecene Copolymer, Styrene/Acrylates Copolymer, Triethoxycaprylylsilane, Aluminum Hydroxide, Xanthan Gum, Stearic Acid, Trisiloxane, Polyester-7, Phenoxyethanol, Polyhydroxystearic Acid, Caprylyl Glycol, Ethylhexylglycerin, Neopentyl Glycol Diheptanoate, Behenyl Alcohol, Tocopheryl Acetate, Disodium EDTA, Silica

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

NEW LOOK

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

ULTRA

SHEER ®

Dry-Touch

Sunscreen

MINERAL SENSITIVE SKIN

BROAD SPECTRUM SPF 30

Antioxidant Vitamin E

100% Mineral Actives

Lightweight clean feel

with PURESCREEN+®

Water resistant (80 minutes)

3.0 FL OZ (88 mL)

69968-0892-1

NEUTROGENA ULTRA SHEER DRY-TOUCH SUNSCREEN BROAD SPECTRUM SPF 30
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0892
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	180 mg in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	66 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ISOHEXADECANE (UNII: 918X1OUF1E)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
DOCOSANOL (UNII: 9G1OE216XY)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE (UNII: 92RU3N3Y1O)
TRISILOXANE (UNII: 9G1ZW13R0G)
PEG-100 STEARATE (UNII: YD01N1999R)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
STEARIC ACID (UNII: 4ELV7Z65AP)
POLYESTER-7 (UNII: 0841698D2F)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69968-0892-3	88 mL in 1 TUBE; Type 0: Not a Combination Product	07/01/2024
2	NDC:69968-0892-1	12 in 1 TRAY	07/01/2024
2		14 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	07/01/2024

Labeler - Johnson & Johnson Consumer Inc. (118772437)