Label: DR.JART EVERY SUN DAY SUN FLUID- homosalate, octinoxate, octisalate, octocrylene, avobenzone liquid
- NDC Code(s): 49404-144-02
- Packager: Have & Be Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 20, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
DOSAGE & ADMINISTRATION
- Apply liberally 15 minutes before sun exposure.
- Use a water resistant sunscreen if swimming or sweating
- Reapply at least every 2 hours.
- 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 - 2 pm
– Wear long-sleeved shirts, pants, hats and
sunglasses- Children under 6 months: Ask a doctor
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
INACTIVE INGREDIENT
WATER, PROPANEDIOL, ALCOHOL, BENZOTRIAZOLYL DODECYL P-CRESOL, PENTYLENE GLYCOL, 1,2-HEXANEDIOL, SILICA, DIMETHICONE/VINYL DIMETHICONECROSSPOLYMER, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VPCOPOLYMER, STYRENE/ACRYLATES COPOLYMER, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, ETHYLHEXYLGLYCERIN, HYDROXYPROPYL METHYLCELLULOSESTEAROXY ETHER, POLYACRYLATE CROSSPOLYMER-6, BUTYLENE GLYCOL, BHT, T-BUTYL ALCOHOL, TOCOPHEROL
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR.JART EVERY SUN DAY SUN FLUID
homosalate, octinoxate, octisalate, octocrylene, avobenzone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49404-144 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 mg in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4 mg in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.9 mg in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 mg in 100 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6.8 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) ALCOHOL (UNII: 3K9958V90M) BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X) PENTYLENE GLYCOL (UNII: 50C1307PZG) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) LAVENDER OIL (UNII: ZBP1YXW0H8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49404-144-02 1 in 1 CARTON 10/31/2019 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 10/31/2019 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(49404-144)
