DR.JART EVERY SUN DAY SUN FLUID- homosalate, octinoxate, octisalate, octocrylene, avobenzone liquid

DR.JART EVERY SUN DAY SUN FLUID by

Drug Labeling and Warnings

DR.JART EVERY SUN DAY SUN FLUID by is a Otc medication manufactured, distributed, or labeled by Have & Be Co., Ltd., Kolmar Korea Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 2.9%
Homosalate 9.0%
Octinoxate 6.8%
Octisalate 4.5%
Octocrylene 4.0%

Purpose

Sunscreen

Use

■ Helps prevent sunburn

Warnings

For external use only

Do not use

on damaged or broken skin

Stop use

and ask a doctor if rash occurs

When using this product

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ Apply liberally 15 minutes before sun exposure
■ Reapply at least every two 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 am
to 2 pm
* wear long-sleeved shirts, pants, hats, and
sunglasses
■ Children under 6 months of age: ask a doctor

Inactive ingredients

WATER\AQUA\EAU,
PROPANEDIOL, ALCOHOL
DENAT., BENZOTRIAZOLYL
DODECYL P-CRESOL,
PENTYLENE GLYCOL,
1,2-HEXANEDIOL, SILICA,
DIMETHICONE/VINYL
DIMETHICONE CROSSPOLYMER,
AMMONIUM
ACRYLOYLDIMETHYLTAURATE/
VP COPOLYMER,
STYRENE/ACRYLATES
COPOLYMER, LAVANDULA
ANGUSTIFOLIA (LAVENDER) OIL,
ETHYLHEXYLGLYCERIN,
HYDROXYPROPYL
METHYLCELLULOSE STEAROXY
ETHER, POLYACRYLATE
CROSSPOLYMER-6, BUTYLENE
GLYCOL, LINALOOL, LIMONENE,
BHT, T-BUTYL ALCOHOL,
TOCOPHEROL <ILN50939>

Other information

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

PRINCIPAL DISPLAY PANEL

Dr.Jart+

Every Sun Day

Sun Fluid

UVA/UVB Protection

Broad Spectrum

SPF 50+

Sunscreen

100 mL / 3.38fl. oz.

INGREDIENTS AND APPEARANCE

DR.JART EVERY SUN DAY SUN FLUID 
homosalate, octinoxate, octisalate, octocrylene, avobenzone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49404-154
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	68 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	40 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	90 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	29 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
TOCOPHEROL (UNII: R0ZB2556P8)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALCOHOL (UNII: 3K9958V90M)
BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PROPANEDIOL (UNII: 5965N8W85T)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LAVENDER OIL (UNII: ZBP1YXW0H8)
HYPROMELLOSE 2208 0.45% STEAROXY ETHER (UNII: MG58AH4FJ8)
WATER (UNII: 059QF0KO0R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49404-154-01	1 in 1 CARTON	12/22/2022
1		100 mL in 1 CONTAINER; 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	12/22/2022

Labeler - Have & Be Co., Ltd. (690400408)

Registrant - Estee Lauder Companies Inc. (790802086)

Establishment
Name	Address	ID/FEI	Business Operations
Kolmar Korea Co., Ltd.		963271750	manufacture(49404-154)