NEUTROGENA MINERAL ULTRA SHEER FACE SPF 70- titanium dioxide, zinc oxide lotion

Neutrogena Mineral Ultra Sheer Face SPF 70 by

Drug Labeling and Warnings

Neutrogena Mineral Ultra Sheer Face SPF 70 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
Titanium Dioxide (6.6%) Zinc Oxide (14.4%)	Sunscreen 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

Inactive ingredients

Water, Caprylic/Capric Triglyceride, Glycerin, Butyloctyl Salicylate, Ethylhexyl Methoxycrylene, VP/Hexadecene Copolymer, Dimethicone, Steareth-21, Calcium Sodium Borosilicate, Triacontanyl PVP, Polyhydroxystearic Acid, Aluminum Hydroxide, Stearic Acid, Triethoxycaprylylsilane, Cetearyl Olivate, Phenoxyethanol, Sodium Chloride, Xanthan Gum, Ethylhexylglycerin, Sorbitan Olivate, Chlorphenesin, Caprylyl Glycol, Tocopheryl Acetate, Disodium EDTA

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 40 mL Carton Label

NEW

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

ULTRA

SHEER ®

Face Liquid

Sunscreen

MINERAL SENSITIVE SKIN

70

BROAD SPECTRUM SPF 70

Antioxidant Vitamin E

Ultra Lightweight

Invisible Finish

All-Day Hydration

1.4 FL OZ (40 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA MINERAL ULTRA SHEER FACE SPF 70 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0895
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	144 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	66 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
DIMETHICONE (UNII: 92RU3N3Y1O)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CHLORPHENESIN (UNII: I670DAL4SZ)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)
SORBITAN OLIVATE (UNII: MDL271E3GR)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
STEARETH-21 (UNII: 53J3F32P58)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0895-1	1 in 1 CARTON	09/06/2024
1		40 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 69968-0895-2	24 in 1 TRAY	09/06/2024
2		1.4 mL in 1 POUCH; 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	09/06/2024

Labeler - Kenvue Brands LLC (118772437)