FDA.reportPublic FDA data

sheer

Manufacturer
HARRIS TEETER | Consumer Product Partners, LLC
Effective date
2024-09-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:54:50

Label at a glance#

Productsheer
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure13 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 liberaly 15 minutes before sun exposure apply to all skin exposed to the sun 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 Broad Spectrum SPF value of 15 or higher and other sun protection...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 12%

Octisalate 5%

Octocrylene 10%

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

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.  Rinse with water to remove

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberaly 15 minutes before sun exposure
  • apply to all skin exposed to the sun
  • 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especialy 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

OTHER SAFETY INFORMATION

  • protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, styrene/acrylates copolymer, silica, butyloctyl salicylate, diethylhexyl 2,6-naphthalate, VP/hexadecene copolymer, glyceryl stearate, PEG-100 stearate, behenyl alcohol, dimethicone, caprylyl methicone, trimethylsiloxysilicate, sodium polyacrylate, chlorphenesin, benzyl alcohol, glycerin, xanthan gum, fragrance, disodium EDTA, BHT

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics or surfaces

*Oxybenzone and octinoxate free

**This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., distributor of Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 55.

Proudly Distributed By: Harris Teeter, LLC
Matthews, NC 28105
1-800-432-6111 or harristeeter.com

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Harris Teeter

Compare to Neutrogena Ultra Sheer Dry-Touch Sunscreen**

Sheer Touch Sunscreen Lotion

BROAD SPECTRUM SPF 55

Water Resistant (80 minutes)

Lightweight formula

Dermatologist tested

REEF FRIENDLY

BPA Free

TOGETHER IN EDUCATION

3 FL OZ (88 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72036-92072036-920-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW)5Z4DPO246AIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
DOCOSANOL9G1OE216XYIACT
DIMETHICONE92RU3N3Y1OIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
TRIMETHYLSILOXYSILICATE (M/Q 0.8-1.0)25LXE464L2IACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
CHLORPHENESINI670DAL4SZIACT
BENZYL ALCOHOLLKG8494WBHIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
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
25039e0e-1bae-a979-e063-6394a90af1d7816a02fb-a00d-4d01-8c5d-56abd6712f9b2024-10-21WarningsExact identifier
spl set id: 816a02fb-a00d-4d01-8c5d-56abd6712f9b

Reported adverse events (FAERS/openFDA)#

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