FDA.reportPublic FDA data

Neutrogena Invisible Daily Defense Face Mist Sunscreen Broad Spectrum SPF 50

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2023-01-24
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:39:10

Label at a glance#

ProductNeutrogena Invisible Daily Defense Face Mist Sunscreen Broad Spectrum SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure10 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

Shake well before use. Spray liberally and spread evenly by hand 15 minutes before sun exposure Hold container 4-6 inches from the skin to apply. Rub in. Do not spray directly onto face. Spray on hands and then apply to face. Rub in. Do not apply in windy conditions. reapply: after 40 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun Protection Measures. Spending time in the...

Storage and handling

protect this product from excessive heat and direct sun May stain some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Avobenzone 3%Sunscreen
Homosalate 10%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 10%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

SPL UNCLASSIFIED SECTION

Flammable keep away from fire and Flame

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • 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

  • Shake well before use.
  • Spray liberally and spread evenly by hand 15 minutes before sun exposure
    Hold container 4-6 inches from the skin to apply. Rub in.
  • Do not spray directly onto face. Spray on hands and then apply to face. Rub in.
  • Do not apply in windy conditions.
  • reapply:
    • after 40 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

STORAGE AND HANDLING SECTION

  • protect this product from excessive heat and direct sun
  • May stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

SD Alcohol 40-B, Dimethicone, Trisiloxane, Diisopropyl Adipate, Acrylates/Octylacrylamide Copolymer, Acrylates/Dimethicone Copolymer, Tocopheryl Acetate, Fragrance, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice

Questions?

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Invisible Daily

defense

face mist

sunscreen

BROAD SPECTRUM

SPF 50

50

sun + antioxidants

oxybenzone free

water resistant (40 minutes)

3.4 FL OZ (100 mL)

Ntg_001Ntg_001

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-068569968-0685-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
TRISILOXANE9G1ZW13R0GIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW)JU3XHR8VWKIACT
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMERV5RS026Q0HIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FEVERFEWZ64FK7P217IACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

Source Document#

Source XML

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
f3080b43-b10b-41a4-e053-2995a90a9419d19bc581-5cf9-44a1-95e5-72246dfa403b2023-01-24WarningsExact identifier
spl id: f3080b43-b10b-41a4-e053-2995a90a9419
spl set id: d19bc581-5cf9-44a1-95e5-72246dfa403b

Reported adverse events (FAERS/openFDA)#

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