Label: INNISFREE DAILY UV DEFENSE SUNSCREEN- avobenzone, homosalate, and octisalate lotion lotion
- NDC Code(s): 71220-086-08, 71220-086-40, 71220-086-41, 71220-086-99
- Packager: Innisfree Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2025
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENTS
- Purpose
- Uses
- Warnings
-
Directions
- Apply liberally 15 minutes before sun exposure.
- 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 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.
-
Inactive ingredients
WATER / AQUA / EAU, BUTYLOCTYL SALICYLATE, ETHYLHEXYL SALICYLATE, BUTYLENE GLYCOL, ETHYLHEXYL METHOXYCRYLENE, BUTYL METHOXYDIBENZOYLMETHANE, ARACHIDYL ALCOHOL, BEHENYL ALCOHOL, POLYMETHYLSILSESQUIOXANE, 1,2-HEXANEDIOL, CETYL ALCOHOL, ARACHIDYL GLUCOSIDE, PHENOXYETHANOL, PROPANEDIOL, POLYACRYLATE CROSSPOLYMER-6, OCTYLDODECANOL, GLYCERYL STEARATE, PEG-100 STEARATE, FRAGRANCE / PARFUM, XANTHAN GUM, LIMONENE, CENTELLA ASIATICA EXTRACT, PORTULACA OLERACEA EXTRACT, ECHIUM PLANTAGINEUM SEED OIL, T-BUTYL ALCOHOL, CAMELLIA SINENSIS LEAF EXTRACT, LINALOOL, ETHYLHEXYLGLYCERIN, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES, CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT, TOCOPHEROL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, GLYCERIN, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT, CITRUS UNSHIU PEEL EXTRACT, OPUNTIA COCCINELLIFERA FRUIT EXTRACT, ORCHID EXTRACT, CAMELLIA JAPONICA LEAF EXTRACT, CITRIC ACID, SODIUM BENZOATE, POTASSIUM SORBATE
- Other information
- Questions?
- Innisfree Daily UV Defense
- Innisfree Daily UV Defense 100mL
- Innisfree Best Seller Mini set - Daily UV Defense 50 mL
- PRINCIPAL DISPLAY PANEL
- Innisfree Brighten+Protect set -- Daily UV Defense 25mL
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INGREDIENTS AND APPEARANCE
INNISFREE DAILY UV DEFENSE SUNSCREEN
avobenzone, homosalate, and octisalate lotion lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71220-086 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 1.25 g in 50 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 3.5 g in 50 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.15 g in 50 mL Inactive Ingredients Ingredient Name Strength OCTYLDODECANOL (UNII: 461N1O614Y) ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW) LINALOOL, (+/-)- (UNII: D81QY6I88E) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TOCOPHEROL (UNII: R0ZB2556P8) GLYCERIN (UNII: PDC6A3C0OX) CYCNOCHES COOPERI FLOWERING TOP (UNII: B9BV87G0K5) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) CETYL ALCOHOL (UNII: 936JST6JCN) PROPANEDIOL (UNII: 5965N8W85T) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) PEG-100 STEARATE (UNII: YD01N1999R) LIMONENE, (+)- (UNII: GFD7C86Q1W) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SUNFLOWER OIL UNSAPONIFIABLES (UNII: T7ZE2WA4MB) SUNFLOWER OIL (UNII: 3W1JG795YI) CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR) TANGERINE PEEL (UNII: JU3D414057) OPUNTIA COCHENILLIFERA FRUIT (UNII: 838ZTK02KH) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) CAMELLIA JAPONICA LEAF (UNII: 4E3VE6KTLY) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) XANTHAN GUM (UNII: TTV12P4NEE) PURSLANE (UNII: M6S840WXG5) DOCOSANOL (UNII: 9G1OE216XY) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71220-086-08 1 in 1 BOX 02/01/2024 09/15/2027 1 50 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:71220-086-40 1 in 1 BOX 07/01/2024 09/17/2027 2 100 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:71220-086-41 1 in 1 BOX 07/01/2024 03/05/2027 3 10 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:71220-086-99 1 in 1 BOX 07/01/2024 12/16/2026 4 25 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 02/01/2024 09/17/2027 Labeler - Innisfree Corporation (557822425) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co., Ltd 963271745 manufacture(71220-086)
