FDA.reportPublic FDA data

Garnier Ombrelle Ultra Light Advanced 30

Manufacturer
L'OREAL USA PRODUCTS INC | L'OREAL USA, INC
Effective date
2024-01-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:12:02

Label at a glance#

ProductGarnier Ombrelle Ultra Light Advanced 30
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure5 sections

Dosage and administration

Adults and children over 6 months and up. Apply generously and evenly 15 minutes before sun exposure. Reapply at least every 2 hours, use a water resistant sunscreen if swimming or sweating.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 5%

Oxbenzone 3%

Warnings

WARNINGS SECTION

For external use only. When using this product avoid contact with eyes. If contact occurs, rinse thoroughlly with water. Do not use on broken skin. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed get medical help or contact a poison control center right away. 

Directions 

DOSAGE & ADMINISTRATION SECTION

Adults and children over 6 months and up. Apply generously and evenly 15 minutes before sun exposure. Reapply at least every 2 hours, use a water resistant sunscreen if swimming or sweating.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cyclopentasiloxane, dicaprylyl ether, alcohol denat., silica, dimethicone, styrene/acrylates copolymer, PEG-30 dipolyhydroxystearate, cyclohexasiloxane, polymethylsilsesquioxane, nylon-12, dicaprylyl carbonate, phenoxyethanol, lauryl PEG/PPG-18/18 methicone, sodium chloride, caprylyl glycol, PEG-8 laurate, methylparaben, poly c10-30 alkyl acrylate, disteardimonium hectorite, isostearyl alcohol. disodium EDTA, dodecane, poloxamer 407, tocopherol, sodium dodecylbenzenesulfonate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-65649967-656-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OXYBENZONE95OOS7VE0YACTIB
WATER059QF0KO0RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALCOHOL3K9958V90MIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
DICAPRYLYL ETHER77JZM5516ZIACT
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW)5Z4DPO246AIACT
PEG-30 DIPOLYHYDROXYSTEARATE9713Q0S7FOIACT
DIMETHICONE92RU3N3Y1OIACT
CYCLOMETHICONE 6XHK3U310BAIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
NYLON-12446U8J075BIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
PHENOXYETHANOLHIE492ZZ3TIACT
LAURYL PEG/PPG-18/18 METHICONEZJ5S27D9NXIACT
SODIUM CHLORIDE451W47IQ8XIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PEG-8 LAURATE762O8IWA10IACT
METHYLPARABENA2I8C7HI9TIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
ISOSTEARYL ALCOHOLQ613OCQ44YIACT
EDETATE DISODIUM7FLD91C86KIACT
DODECENEWYE669F3GRIACT
POLOXAMER 407TUF2IVW3M2IACT
TOCOPHEROLR0ZB2556P8IACT
SODIUM DODECYLBENZENESULFONATE554127163YIACT

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
c2f97c9a-51d3-49df-9ba1-66e3e06027ce633e5269-46ba-40d6-892c-53ba759f38d82024-01-31WarningsExact identifier
spl id: c2f97c9a-51d3-49df-9ba1-66e3e06027ce
spl set id: 633e5269-46ba-40d6-892c-53ba759f38d8

Reported adverse events (FAERS/openFDA)#

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