NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide, zinc oxide lotion 
Johnson & Johnson Consumer Inc.

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Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30

Drug Facts

Active ingredientsPurpose
Titanium Dioxide (4.9%)Sunscreen
Zinc Oxide (21.6%)Sunscreen

Uses

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

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

Distributed by:

JOHNSON & JOHNSON CONSUMER INC.

Skillman, NJ 08558

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)

Neutrogena_01

NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0815
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE49 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE216 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0815-11 in 1 CARTON08/21/2023
140 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69968-0815-224 in 1 TRAY01/01/2024
21.4 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02008/21/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 12/2023
Document Id: 0c360d65-f12f-fc61-e063-6294a90a3a3b
Set id: 003123d2-9675-fdd2-e063-6294a90a0130
Version: 2
Effective Time: 20231211
 
Johnson & Johnson Consumer Inc.