DR.JART EVERY SUN DAY SUN FLUID- homosalate, octinoxate, octisalate, octocrylene, avobenzone liquid 
Have & Be Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

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

Principal Display PanelDr.Jart+

Every Sun Day

Sun Fluid

UVA/UVB Protection

Broad Spectrum

SPF 50+

Sunscreen

100 mL / 3.38fl. oz.

DR.JART EVERY SUN DAY SUN FLUID 
homosalate, octinoxate, octisalate, octocrylene, avobenzone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49404-154
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE90 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE29 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE45 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE68 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
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)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49404-154-011 in 1 CARTON12/22/2022
1100 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35212/22/2022
Labeler - Have & Be Co., Ltd. (690400408)
Registrant - Have & Be Co., Ltd. (690400408)
Establishment
NameAddressID/FEIBusiness Operations
Kolmar Korea Co., Ltd.689512611manufacture(49404-154)

Revised: 12/2022
Document Id: f06d8f90-f3e0-6d76-e053-2a95a90af1f8
Set id: f06d8f90-f3df-6d76-e053-2a95a90af1f8
Version: 1
Effective Time: 20221222
 
Have & Be Co., Ltd.