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

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 productis 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

Every Sun Day
Sun Fluid

UVA/UVB Protection

Broad Spectrum

SPF 50+

100 mL / 3.38 fl. oz.

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49404-307
Route of Administration	TOPICAL

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

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49404-307-01	1 in 1 CARTON	08/11/2023
1		100 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	M020	08/11/2023

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

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
HK Kolmar Canada, Inc		243501959	manufacture(49404-307)