FDA.reportPublic FDA data

Neutrogena Ultra Sheer Dry Touch

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2020-10-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:12:30

Label at a glance#

ProductNeutrogena Ultra Sheer Dry Touch Sunscreen Broad Spectrum SPF 55
Active ingredientAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
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 liberally 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...

Storage and handling

protect this product from excessive heat and direct sun protect from freezing ship with winter protection may stain some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 2.8%, Oxybenzone 6%

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

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

  • apply liberally 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

STORAGE AND HANDLING SECTION

  • protect this product from excessive heat and direct sun
  • protect from freezing
  • ship with winter protection
  • may stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butyloctyl salicylate, caprylyl Methicone, Behenyl Alcohol, VP/hexadecene copolymer, BHT, Methylparaben, trimethylsiloxysilicate, Propylparaben, Diethylhexyl 2,6-Naphthalate, Dimethicone, sodium polyacrylate, Disodium EDTA, Ethylhexyl Stearate, Ethylhexylglycerin, Fragrance, Glyceryl Stearate, PEG-100 Stearate, Phenoxyethanol, Silica, Ethylparaben, Iodopropynyl butylcarbamate, Trideceth-6, Water, Xanthan Gum

Questions?

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 - 147 mL Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VALUE-SIZE
Neutrogena®

Ultra Sheer®
DRY-TOUCH
SUNSCREEN
Broad Spectrum SPF 55

55

helioplex®
broad spectrum uva-uvb

LIGHTWEIGHT
CLEAN FEEL

fast absorbing
water resistant (80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

5 FL OZ (147 mL)

PRINCIPAL DISPLAY PANEL - 147 mL Tube Label
PRINCIPAL DISPLAY PANEL - 147 mL Tube Label

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-039169968-0391-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
AvobenzoneG63QQF2NOXACTIB
HomosalateV06SV4M95SACTIB
Octisalate4X49Y0596WACTIB
Octocrylene5A68WGF6WMACTIB
Oxybenzone95OOS7VE0YACTIB
Butyloctyl salicylate2EH13UN8D3IACT
DOCOSANOL9G1OE216XYIACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
MethylparabenA2I8C7HI9TIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
PropylparabenZ8IX2SC1OHIACT
Diethylhexyl 2,6-NaphthalateI0DQJ7YGXMIACT
Dimethicone92RU3N3Y1OIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
Ethylhexyl StearateEG3PA2K3K5IACT
Ethylhexylglycerin147D247K3PIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 StearateYD01N1999RIACT
PhenoxyethanolHIE492ZZ3TIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ethylparaben14255EXE39IACT
Iodopropynyl butylcarbamate603P14DHEBIACT
Trideceth-63T5PCR2H0CIACT
Water059QF0KO0RIACT
Xanthan GumTTV12P4NEEIACT

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
3b8d26e4-e80d-401f-80f7-36bc54364ad76ef7d10d-16b2-4f77-9348-e66831c8353f2020-10-02WarningsExact identifier
spl id: 3b8d26e4-e80d-401f-80f7-36bc54364ad7
spl set id: 6ef7d10d-16b2-4f77-9348-e66831c8353f

Reported adverse events (FAERS/openFDA)#

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