FDA.reportPublic FDA data

Neutrogena sensitive skin face Liquid

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2023-01-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:41:23

Label at a glance#

ProductNeutrogena sensitive skin face Liquid Sunscreen Broad Spectrum SPF50
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure11 sections

Indications and 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

Dosage and administration

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 value of SPF of 15 or higher and other sun protection measures including: Limit time in...

Storage and handling

Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 4.9%
Zinc Oxide 2.9%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 value of SPF 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 age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Questions or comments?

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 40 mL Bottle Blister Pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neutrogena ®

sensitive skin
face
LIQUID SUNSCREEN
Broad Spectrum
SPF50

100%
naturally sourced
sunscreen ingredients

layers invisibly
under makeup

ultra-light liquid
formula
water resistant
(80 minutes)

pureSCREEN ®
broad spectrum uva•uvb

1.4 FL OZ (40mL)

#1 DERMATOLOGIST RECOMMENDED SUNCARE

PRINCIPAL DISPLAY PANEL - 40 mL Bottle Blister Pack
PRINCIPAL DISPLAY PANEL - 40 mL Bottle Blister Pack

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-033469968-0334-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
LEVOMENOL24WE03BX2TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CAPRYLYL GLYCOL00YIU5438UIACT
DIMETHICONE92RU3N3Y1OIACT
DMDM HYDANTOINBYR0546TOWIACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
PPG-12/SMDI COPOLYMER1BK9DDD24EIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
TRISILOXANE9G1ZW13R0GIACT
WATER059QF0KO0RIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
015f76af-1adf-bf1b-e063-6394a90ac7c3abc65cd6-e230-4867-8902-c2bf5e2e62b32023-07-26WarningsExact identifier
spl set id: abc65cd6-e230-4867-8902-c2bf5e2e62b3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.