LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g by DONGDONGGURIMOO CO.,LTD. / KONAD CO.,LTD.

LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g by

Drug Labeling and Warnings

LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g by is a Otc medication manufactured, distributed, or labeled by DONGDONGGURIMOO CO.,LTD., KONAD CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50G- avobenzone, homosalate, octinoxate, octocrylene, octisalate lotion 
DONGDONGGURIMOO CO.,LTD.

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Active ingredients

avobenzone 3.0%

Homosalate 10.0%

Octinoxate 7.0%

Octocrylene 10.0%

Octisalate 5.0%

Purpose

SUNSCREEN

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

Warnings

For external use only

Do not use

on damaged skin or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

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

■ 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

■ 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

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

LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50G 
avobenzone, homosalate, octinoxate, octocrylene, octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85948-250
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.5 g  in 50 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	3.5 g  in 50 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 50 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.5 g  in 50 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
POLYGLYCERYL-6 BEHENATE (UNII: 4T2L7QI313)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ADENOSINE (UNII: K72T3FS567)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
MONARDA DIDYMA LEAF (UNII: JY15982UBB)
ROSEMARY (UNII: IJ67X351P9)
ASIATICOSIDE (UNII: PKO39VY215)
MADECASSIC ACID (UNII: M7O1N24J82)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
NIACINAMIDE (UNII: 25X51I8RD4)
DOCOSANOL (UNII: 9G1OE216XY)
POLYSORBATE 60 (UNII: CAL22UVI4M)
POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T)
PANTHENOL (UNII: WV9CM0O67Z)
SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
MADECASSOSIDE (UNII: CQ2F5O6YIY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85948-250-02	1 in 1 BOX	01/12/2026	04/02/2026
1	NDC: 85948-250-01	1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/12/2026	04/02/2026

Labeler - DONGDONGGURIMOO CO.,LTD. (690411575)

Establishment
Name	Address	ID/FEI	Business Operations
KONAD CO.,LTD.		688329887	manufacture(85948-250)

Revised: 4/2026

Document Id: 4e75cc73-4c55-7f61-e063-6294a90a987d

34390-5

Set id: 4830cf3e-6e77-d312-e063-6294a90a5133

Version: 2

Effective Time: 20260402