INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN- zinc oxide lotion lotion 
Innisfree Corporation

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innisfree Daily UV Defense Mineral Sunscreen

Drug Facts

ACTIVE INGREDIENTS

Zinc Oxide 17%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use on damanged 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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

- Limit time in the sun, especially from 10 a.m. - 2 p.m.

- Wear long-sleeved shirts, pants, hats, and sunglasses.

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

Protect the product in this container from excessive heat and direct sun

Questions?

support@us.amorepacific.com

Innisfree Daily UV Defense

Innisfree

DAILY

UV DEFENSE

MINERAL

SUNSCREEN

BROAD SPECTRUM

SPF 45

Color-correcting

Satin Finish

50mL 1.69Fl.Oz.

50ml mineral

INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN 
zinc oxide lotion lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71220-087
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE8 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71220-087-081 in 1 BOX02/01/2024
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02002/01/2024
Labeler - Innisfree Corporation (557822425)

Revised: 1/2024
Document Id: 0f19e26b-bfec-26dc-e063-6394a90ad9e8
Set id: 0e9cd3e5-cff8-7594-e063-6394a90aad90
Version: 2
Effective Time: 20240116
 
Innisfree Corporation