Label: LANEIGE HYDRO UV DEFENSE EX BROAD SPECTRUM SPF 50- octocrylene, homosalate, octisalate, avobenzone cream
- NDC Code(s): 43419-791-08
- Packager: AMOREPACIFIC CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 8, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Uses
- Warnings
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Directions
Apply liberally 15 minutes before sun exposure.
Children under 6 months of age: Ask a doctor.
Reapply at least every 2 hours.
Use a water-resistant sunscreen if swimming or sweating.
Sun Protection Measures. Spending time in the sun increases your rick 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.
- Other information
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Inactive ingredients
WATER, PROPANEDIOL, BUTYLOCTYL SALICYLATE, GLYCERIN, DIPHENYLSILOXY PHENYL TRIMETHICONE, SILICA, PHENYL TRIMETHICONE, CAPRYLYL METHICONE, BEHENYL ALCOHOL, VP/EICOSENE COPOLYMER, TRIMETHYLSILOXYSILICATE, C14-22 ALCOHOLS, GLYCERYL STEARATE, PEG-100 STEARATE, 1,2-HEXANEDIOL, CETYL ALCOHOL, POTASSIUM CETYL PHOSPHATE, POLYACRYLATE-13, POLYISOBUTENE, C12-20 ALKYL GLUCOSIDE, ETHYLHEXYLGLYCERIN, FRAGRANCE / PARFUM, DISODIUM EDTA, POLYSORBATE 20, SORBITAN ISOSTEARATE, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER WATER, BUTYLENE GLYCOL, ALOE BARBADENSIS LEAF EXTRACT, PENTYLENE GLYCOL, CENTELLA ASIATICA FLOWER/LEAF/STEM EXTRACT, BRASSICA OLERACEA ITALICA (BROCCOLI) EXTRACT, HIBISCUS ABELMOSCHUS EXTRACT, TOCOPHEROL, MAGNESIUM SULFATE, CALCIUM CHLORIDE, XANTHAN GUM, CITRIC ACID, SODIUM BENZOATE, POTASSIUM SORBATE, MANGANESE SULFATE, CHENOPODIUM QUINOA SEED EXTRACT, ZINC SULFATE, ASCORBYL GLUCOSIDE
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- LANEIGE HYDRO UV DEFENSE EX
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INGREDIENTS AND APPEARANCE
LANEIGE HYDRO UV DEFENSE EX BROAD SPECTRUM SPF 50
octocrylene, homosalate, octisalate, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43419-791 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 3.5 g in 50 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 1.25 g in 50 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4.5 g in 50 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.25 g in 50 mL Inactive Ingredients Ingredient Name Strength CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X) ABELMOSCHUS MOSCHATUS FLOWER (UNII: 599O6K8K81) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) DOCOSANOL (UNII: 9G1OE216XY) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CENTELLA ASIATICA FLOWERING TOP (UNII: J02K2IV2PB) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM BENZOATE (UNII: OJ245FE5EU) ZINC SULFATE MONOHYDRATE (UNII: PTX099XSF1) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) POLYSORBATE 20 (UNII: 7T1F30V5YH) C14-22 ALCOHOLS (UNII: B1K89384RJ) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) MANGANESE SULFATE (UNII: W00LYS4T26) CETYL ALCOHOL (UNII: 936JST6JCN) POLYACRYLATE-13 (UNII: FS2D4T67EA) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GLYCERIN (UNII: PDC6A3C0OX) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) LAVENDER OIL (UNII: ZBP1YXW0H8) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ALOE VERA LEAF (UNII: ZY81Z83H0X) PENTYLENE GLYCOL (UNII: 50C1307PZG) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43419-791-08 1 in 1 BOX 05/01/2024 1 50 mL in 1 TUBE; 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 05/01/2024 Labeler - AMOREPACIFIC CORPORATION (631035289)
