NEUTROGENA SENSITIVE SKIN FACE MINERAL SUNSCREEN BROAD SPECTRUM SPF 50- titanium dioxide and zinc oxide lotion 
Johnson & Johnson Consumer Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neutrogena ® Sensitive Skin face mineral sunscreen BROAD SPECTRUM SPF 50

Drug Facts

Active ingredients

Titanium Dioxide (4.9%), Zinc Oxide (2.9%)

Purpose

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
  • a small amount of grittiness may be expected

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Dimethicone, Trisiloxane, Styrene/Acrylates Copolymer, Silica, Cetyl PEG/PPG-10/1 Dimethicone, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, PPG-12/SMDI Copolymer, Bisabolol, Aluminum Hydroxide, Caprylyl Glycol, Stearic Acid, Magnesium Sulfate, DMDM Hydantoin, Triethoxycaprylylsilane, BHT

Questions?

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 - 40 mL Blister Pack Bottle Label

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Sensitive Skin

Face

mineral sunscreen

BROAD SPECTRUM

SPF 50

50

100%

mineral active

ingredients

layers invisibly

under makeup

ultra-light liquid

formula

water resistant

(80 minutes)

1.4 FL OZ (40 mL)

ntg001

NEUTROGENA SENSITIVE SKIN FACE MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0624
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 OXIDE29 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)  
LEVOMENOL (UNII: 24WE03BX2T)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0624-11 in 1 BLISTER PACK01/31/202001/01/2024
140 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/31/202001/01/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 7/2023
Document Id: 015fbc96-a74c-5d4c-e063-6294a90a6ab0
Set id: a4ad5145-6bdb-4af5-bc4f-d1f0352310aa
Version: 6
Effective Time: 20230726
 
Johnson & Johnson Consumer Inc.