LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g

Manufacturer
DONGDONGGURIMOO CO.,LTD. | KONAD CO.,LTD.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:53:07

Label at a glance#

ProductLEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g
Active ingredientAVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE, OCTISALATE
Label structure12 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 liberally 15 minutes before sun exposure. 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 ■ ch...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

avobenzone 3.0%

Homosalate 10.0%

Octinoxate 7.0%

Octocrylene 10.0%

Octisalate 5.0%

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 skin or broken skin

When using this product

OTC - WHEN USING SECTION

• keep out of eyes. Rinse with water to remove.

Stop use

OTC - STOP USE SECTION

and ask a doctor if • rash occurs

Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ apply liberally 15 minutes before sun exposure.

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

■ reapply at least every 2 hours

■ use a water-resistant sunscreen if swimming or sweating

Other information

OTHER SAFETY INFORMATION

■ protect the product from excessive heat and direct sun ■ Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Butyloctyl Salicylate, Butylene Glycol, Polyglyceryl-6 Stearate, Ethylhexyl Methoxycrylene, Silica, Niacinamide, Poly C10-30 Alkyl Acrylate, Sorbitan Sesquioleate, Behenyl Alcohol, 1,2-Hexanediol, Hydroxyacetophenone, Polysorbate 60, Sodium Polyacryloyldimethyl Taurate, Polyglyceryl-6 Behenate, Tocopheryl Acetate, Panthenol, Polyacrylate Crosspolymer-6, Sphingomonas Ferment Extract, Disodium EDTA, Adenosine, Centella Asiatica Extract, Monarda Didyma Leaf Extract, Mentha Piperita Leaf Extract, Lavandula Angustifolia Flower Extract, Freesia Refracta Extract, Rosmarinus Officinalis Leaf Extract, Chamomilla Recutita Flower Extract, Asiaticoside, Madecassoside, Madecassic Acid, Asiatic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEBELAGE UV SUN ULTRA SHIELD SUN SCREEN LOTIONLEBELAGE UV SUN ULTRA SHIELD SUN SCREEN LOTION

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85948-25085948-250-01, 85948-250-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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
4e75cc73-4c55-7f61-e063-6294a90a987d4830cf3e-6e77-d312-e063-6294a90a51332026-04-02WarningsExact identifier
spl set id: 4830cf3e-6e77-d312-e063-6294a90a5133

Reported adverse events (FAERS/openFDA)#

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