Drug Facts

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA PRODUCTS, INC. | Unette Corporation
Effective date
2026-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:28

Label at a glance#

ProductLa Roche Posay Laboratoire Dermatologique Anthelios Glow Daily Glow Sunscreen Pearl Cell OX Shield Broad Spectrum SPF 35
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

For sunscreen use: ● apply generously 15 minutes before sun exposure ● reapply  at least every 2 hours ● use a water resistant sunscreen if swimming or sweating ● 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: ● lim...

Storage and handling

protect the product in this container from excessive heat and direct sun store at 20 o C - 25 o C (68 o F - 77 o F)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 13%

Octisalate 5%

Octocrylene 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

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 Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

● apply generously 15 minutes before sun exposure

● reapply at least every 2 hours

● use a water resistant sunscreen if swimming or sweating

● 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 the product in this container from excessive heat and direct sun
  • store at 20oC - 25oC (68oF - 77oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, dicaprylyl carbonate,
alcohol denat., synthetic fluorphlogopite,
C12-22 alkyl acrylate/hydroxyethylacrylate
copolymer, dimethicone, silica, zea mays
(corn) starch, titanium dioxide,
phenoxyethanol, dimethicone/PEG-10/15
crosspolymer, hydroxyacetophenone,
pentaerythrityl tetra-di-t-butyl
hydroxyhydrocinnamate, iron oxides,
acrylamide/sodium acryloyldimethyltaurate
copolymer, xanthan gum, arachidyl alcohol,
chlorphenesin, caprylyl glycol,
isohexadecane, behenyl alcohol,
tocopherol, pentylene glycol, tetrasodium
glutamate diacetate, diethylhexyl
syringylidenemalonate, trisodium
ethylenediamine disuccinate, arachidyl
glucoside, citric acid, polysorbate 80, ammonium polyacryloyldimethyl taurate, cassia alata leaf extract,
maltodextrin, sorbitan oleate, tin
oxide, dipropylene glycol, glycine
soja (soybean) oil, caprylic/capric
triglyceride, disodium stearoyl
glutamate, sodium citrate,
aluminum hydroxide

Questions or comments?

OTC - QUESTIONS SECTION

1-888-LRP-LAB0 1-888-577-5226

Monday - Friday (9 a.m. - 5 p.m. EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

40 mL carton40 mL carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codelr.oaqr.io/01/0360600064282940 mL tube.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82046-829-01La Roche Posay Laboratoire Dermatologique Anthelios Glow Daily Glow Sunscreen Pearl Cell OX Shield Broad Spectrum SPF 351 in 1 CARTONLIQUID11
82046-829-01La Roche Posay Laboratoire Dermatologique Anthelios Glow Daily Glow Sunscreen Pearl Cell OX Shield Broad Spectrum SPF 3540 mL in 1 TUBELIQUID401

Products#

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

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82046-82982046-829-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 44 matching rows.

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
La Roche Posay Laboratoire Dermatologique Anthelios Glow Daily Glow Sunscreen Pearl Cell OX Shield Broad Spectrum SPF 35AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENEL'Oreal USA Products Incc6a1b995-1898-4a92-b128-7d5ebd6d8d3d2026-04-28WarningsExact identifier
ndc (package): 82046-829-01
ndc (product): 82046-829
ndc11 (package): 82046082901
spl id: e6cf216c-28d4-4cbc-942d-b9bd2cdde71a
spl set id: c6a1b995-1898-4a92-b128-7d5ebd6d8d3d

Reported adverse events (FAERS/openFDA)#

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