FDA.reportPublic FDA data

MeO UV Clear Sunscreen

Manufacturer
Sage Pharmaceuticals Inc
Effective date
2025-10-03
Label type
HUMAN OTC DRUG LABEL
Version
32920
Source
legacy-cache
Hydrated at
2026-08-01 20:34:18

Label at a glance#

ProductMeO UV Clear Sunscreen
Active ingredientTITANIUM DIOXIDE
Label structure11 sections

Indications and uses

UVA / UVB / HEV protection

Dosage and administration

Apply an appropriate amount to the face and body prior to sun exposure, then pat lightly on the area. Reapply as needed.

Storage and handling

Store in a cool, dry place away from heat and direct sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide   11.3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

UVA / UVB / HEV protection

Directions

DOSAGE & ADMINISTRATION SECTION

Apply an appropriate amount to the face and body prior to sun exposure, then pat lightly on the area. Reapply as needed.

Cautions

WARNINGS SECTION

External use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - STOP USE SECTION

Avoid contact with eyes. In case of severe irritation, stop usage immediately and consult a doctor.

Storage

STORAGE AND HANDLING SECTION

Store in a cool, dry place away from heat and direct sunlight.

SPL UNCLASSIFIED SECTION

Sage Pharmaceuticals, Inc

Product of Taiwan

Distributed by
Beauty River International Group, Inc
901 S. Fremont Ave Suite 108,
Alhambra, CA 91803-4703, USA

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER, TRISILOXANE, PEG-6 CAPRYLIC/CAPRIC GLYCERIDES, COCO-CAPRYLATE/CAPRATE, GLYCERYL STEARATE CITRATE, PENTYLENE GLYCOL,  N-ACETYLGLUCOSAMINE, NIACINAMIDE, DIMETHICONE, SILICON DIOXIDE, PROPANEDIOL, SODIUM ACRYLATES CROSSPOLYMER-2, 1,2-HEXANEDIOL, XANTHAN GUM, BUTYLENE GLYCOL, LECITHIN, SUNFLOWER, CAPRYLHYDROXAMIC ACID, MEDICAGO SATIVA WHOLE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83119-12683119-126-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TRISILOXANE9G1ZW13R0GIACT
PEG-6 CAPRYLIC/CAPRIC GLYCERIDESGO50W2HWO8IACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
PENTYLENE GLYCOL50C1307PZGIACT
N-ACETYLGLUCOSAMINEV956696549IACT
NIACINAMIDE25X51I8RD4IACT
DIMETHICONE92RU3N3Y1OIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PROPANEDIOL5965N8W85TIACT
SODIUM ACRYLATES CROSSPOLYMER-2D3HPR4WW6FIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
XANTHAN GUMTTV12P4NEEIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
LECITHIN, SUNFLOWER834K0WOS5GIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
MEDICAGO SATIVA WHOLEDJO934BRBDIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
403da692-db67-49ca-e063-6394a90ab2b3bc1e070f-86b8-4b6b-aec8-ed2fc6008ef12025-10-03WarningsExact identifier
spl id: 403da692-db67-49ca-e063-6394a90ab2b3
spl set id: bc1e070f-86b8-4b6b-aec8-ed2fc6008ef1

Reported adverse events (FAERS/openFDA)#

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