Label: INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN- zinc oxide lotion lotion
- NDC Code(s): 71220-087-08
- Packager: Innisfree Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 11, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENTS
- Purpose
- Uses
- Warnings
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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.
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Inactive ingredients
WATER / AQUA / EAU, PROPYLHEPTYL CAPRYLATE, BUTYLOCTYL SALICYLATE, PROPANEDIOL, CAPRYLYL METHICONE, DISILOXANE, POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, POLYMETHYLSILSESQUIOXANE, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, TRIETHOXYCAPRYLYLSILANE, 1,2-HEXANEDIOL, SILICA, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, SYNTHETIC FLUORPHLOGOPITE, DICAPRYLYL CARBONATE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, CHROMIUM OXIDE GREENS (CI 77288), MICA, ETHYLHEXYLGLYCERIN, SODIUM HYALURONATE, TOCOPHEROL, SQUALANE, CERAMIDE NP, NIACINAMIDE, HYDROLYZED SODIUM HYALURONATE, PANTHENOL, BUTYLENE GLYCOL, CENTELLA ASIATICA EXTRACT, CENTELLA ASIATICA LEAF EXTRACT, SACCHAROMYCES FERMENT, CENTELLA ASIATICA ROOT EXTRACT, HYDROXYPROPYLTRIMONIUM HYALURONATE, ASIATICOSIDE, MADECASSOSIDE, HYDROLYZED HYALURONIC ACID, SODIUM ACETYLATED HYALURONATE, HYALURONIC ACID, SODIUM HYALURONATE CROSSPOLYMER, POTASSIUM HYALURONATE, ASIATIC ACID, MADECASSIC ACID
- Other information
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- Innisfree Daily UV Defense
-
INGREDIENTS AND APPEARANCE
INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN
zinc oxide lotion lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71220-087 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 8 g in 50 mL Inactive Ingredients Ingredient Name Strength CENTELLA ASIATICA ROOT (UNII: 8MXU1P42J0) MADECASSOSIDE (UNII: CQ2F5O6YIY) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PANTHENOL (UNII: WV9CM0O67Z) PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) MICA (UNII: V8A1AW0880) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SQUALANE (UNII: GW89575KF9) CENTELLA ASIATICA LEAF (UNII: 6810070TYD) HYALURONIC ACID (UNII: S270N0TRQY) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHROMIC OXIDE (UNII: X5Z09SU859) CERAMIDE NP (UNII: 4370DF050B) NIACINAMIDE (UNII: 25X51I8RD4) SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) MADECASSIC ACID (UNII: M7O1N24J82) SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) ASIATIC ACID (UNII: 9PA5A687X5) ASIATICOSIDE (UNII: PKO39VY215) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) PROPANEDIOL (UNII: 5965N8W85T) HEXAMETHYLDISILOXANE (UNII: D7M4659BPU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71220-087-08 1 in 1 BOX 02/01/2024 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 02/01/2024 Labeler - Innisfree Corporation (557822425)