NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide, zinc oxide lotion

Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 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	Purpose
Titanium Dioxide (4.9%)	Sunscreen
Zinc Oxide (21.6%)	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

Shake bottle well before use.

For Sunscreen Use:

apply generously 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, Isononyl Isononanoate, Dicaprylyl Ether, C12-15 Alkyl Benzoate, Polyglyceryl-2 Dipolyhydroxystearate, Propylene Glycol, Dimethicone, Zingiber Officinale (Ginger) Root Extract, Tocopheryl Acetate, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Calcium Sodium Borosilicate, Polyhydroxystearic Acid, Triethoxycaprylylsilane, Sorbitan Sesquioleate, Sodium Chloride, Aluminum Hydroxide, Phenoxyethanol, Triacontanyl PVP, Ethylhexylglycerin, Stearic Acid, Iron Oxides

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 - 40 mL Bottle Label

NEW

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

PURESCREEN+TM

MINERAL

INVISIBLE

DAILY

DEFENSE

FACE LIQUID

30

SUNSCREEN

BROAD SPECTRUM SPF 30

UVA/UVB PROTECTION

sun + environment ∙ invisible finish

antioxidant complex ∙ oxybenzone free

water resistant (80 minutes)

1.4 FL OZ (40 mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0815
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	49 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	216 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GINGER (UNII: C5529G5JPQ)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
STEARIC ACID (UNII: 4ELV7Z65AP)
FERROUS OXIDE (UNII: G7036X8B5H)
FEVERFEW (UNII: Z64FK7P217)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0815-1	1 in 1 CARTON	08/21/2023
1		40 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 69968-0815-2	24 in 1 TRAY	01/01/2024
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	08/21/2023

Labeler - Kenvue Brands LLC (118772437)