FDA.reportPublic FDA data

Garnier Nutritioniste Moisture Rescue Lightweight UV SPF 15

Manufacturer
L'Oreal USA Products Inc
Effective date
2019-09-16
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-02 00:11:33

Label at a glance#

ProductGarnier Nutritioniste Moisture Rescue Lightweight UV SPF 15
Active ingredientEnsulizole, Octinoxate
Label structure9 sections

Indications and uses

Helps prevent sunburn. Higher SPF gives more sunburn protection.

Dosage and administration

Gently apply Moisture Rescue Lightweight UV-Lotion SPF 15 to face and neck daily prior to sun exposure.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ensulizole 1.5%, Octinoxate 7.5%

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn. Higher SPF gives more sunburn protection.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

When using this product

OTC - WHEN USING SECTION

KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

Stop use and consult a doctor

OTC - STOP USE SECTION

IF RASH OR IRRITATION DEVELOPS AND LASTS.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISION CONTROL CENTER RIGHT AWAY.

Directions

DOSAGE FORMS & STRENGTHS SECTION

Gently apply Moisture Rescue Lightweight UV-Lotion SPF 15 to face and neck daily prior to sun exposure.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, allantoin, titanium dioxide, xanthan gum, palmitic acid, methylparaben, ethylparaben, isobutylparaben, butylparaben

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EnsulizoleACTIVE INGREDIENT9YQ9DI1W424
OctinoxateACTIVE INGREDIENT4Y5P7MUD514
EnsulizoleACTIVE MOIETY9YQ9DI1W424
OctinoxateACTIVE MOIETY4Y5P7MUD514

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-45749967-457-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
Ensulizole9YQ9DI1W42ACTIB
Octinoxate4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
STEARIC ACID4ELV7Z65APIACT
XANTHAN GUMTTV12P4NEEIACT
PALMITIC ACID2V16EO95H1IACT
METHYLPARABENA2I8C7HI9TIACT
ETHYLPARABEN14255EXE39IACT
BUTYLPARABEN3QPI1U3FV8IACT
ISOBUTYLPARABEN0QQJ25X58GIACT

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
2f9a8d80-0b25-4ff8-a2c8-c006a9644ce01e8a170b-4a99-4784-a6bb-9e231fc4aa612019-09-16WarningsExact identifier
spl id: 2f9a8d80-0b25-4ff8-a2c8-c006a9644ce0
spl set id: 1e8a170b-4a99-4784-a6bb-9e231fc4aa61

Reported adverse events (FAERS/openFDA)#

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