DR.JART EVERY SUN DAY MINERAL SUN SCREEN- zinc oxide, titanium dioxide cream 
Have & Be Co., Ltd.

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Dr.Jart Every Sun Day Mineral Sun Screen

Zinc Oxide 11.5%

Titanium Dioxide 4.1%

Sunscreen

Helps prevent sunburn

If used as directed with other sun protection meausres (see Directions), decreases the risk of skin cancer and early skin aging casued by the sun

– Limit time in the sun, especially from 10 am - 2 pm

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

For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove.
Stop using and ask a doctor if rash occurs.

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Water, CYCLOPENTASILOXANE, PROPANEDIOL, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, LAURYL POLYGLYCERYL-3POLYDIMETHYLSILOXYETHYL DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, BUTYLOCTYL SALICYLATE, CAPRYLYL METHICONE, 1,2-HEXANEDIOL, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, STEARIC ACID, ALUMINUM HYDROXIDE, POLYGLYCERYL-3, POLYDIMETHYLSILOXYETHYLDIMETHICONE, TRIETHOXYCAPRYLYLSILANE, SORBITAN CAPRYLATE, CITRUS AURANTIUM DULCIS (ORANGE) OIL, GLYCERYL CAPRYLATE, ETHYLHEXYLGLYCERIN, CITRUS NOBILIS (MANDARIN ORANGE) PEEL OIL, LITSEA CUBEBA FRUIT OIL, TOCOPHEROL

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

You may report a serious adverse event from use of this product to: Report Reaction, LLC PO Box 22 Plainsboro, NJ 08536-0222

image description

DR.JART EVERY SUN DAY MINERAL SUN SCREEN 
zinc oxide, titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49404-143
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE2.05 mg  in 50 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION5.75 mg  in 50 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
PROPANEDIOL (UNII: 5965N8W85T)  
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)  
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49404-143-021 in 1 CARTON10/31/2019
150 mL in 1 CONTAINER; Type 0: Not a Combination Product
2NDC:49404-143-035 mL in 1 TUBE; Type 0: Not a Combination Product12/21/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/31/2019
Labeler - Have & Be Co., Ltd. (690400408)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
Kolmar Korea Co., Ltd.963271750manufacture(49404-143)

Revised: 6/2024
Document Id: 1b55294f-1448-bf77-e063-6394a90a837f
Set id: 33356dd9-44c7-485f-814a-518ab1a29a37
Version: 4
Effective Time: 20240620
 
Have & Be Co., Ltd.