Label: DR.JART EVERY SUN DAY MINERAL SUN SCREEN- titanium dioxide, zinc oxide cream
- NDC Code(s): 49404-153-01, 49404-153-02
- Packager: Have & Be Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 4, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
- Warnings
-
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,
CYCLOPENTASILOXANE,
PROPANEDIOL, BUTYLENE
GLYCOL DICAPRYLATE/DICAPRATE,
LAURYL
POLYGLYCERYL-3
POLYDIMETHYLSILOXYETHYL
DIMETHICONE, METHYL
METHACRYLATE
CROSSPOLYMER, BUTYLOCTYL
SALICYLATE, CAPRYLYL
METHICONE, MAGNESIUM
SULFATE, DISTEARDIMONIUM
HECTORITE, 1,2-HEXANEDIOL,
STEARIC ACID,
POLYGLYCERYL-3
POLYDIMETHYLSILOXYETHYL
DIMETHICONE,
TRIETHOXYCAPRYLYLSILANE,
SORBITAN CAPRYLATE,
GLYCERYL CAPRYLATE,
ETHYLHEXYLGLYCERIN, CITRUS
NOBILIS (MANDARIN ORANGE)
PEEL OIL, LITSEA CUBEBA
FRUIT OIL, CITRUS AURANTIUM
DULCIS (ORANGE) OIL,
ALUMINUM HYDROXIDE,
LIMONENE, CITRAL,
TOCOPHEROL <ILN50931> - Other information
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
DR.JART EVERY SUN DAY MINERAL SUN SCREEN
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49404-153 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 41 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 115 mg in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) STEARIC ACID (UNII: 4ELV7Z65AP) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) CITRAL (UNII: T7EU0O9VPP) TOCOPHEROL (UNII: R0ZB2556P8) ORANGE OIL (UNII: AKN3KSD11B) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) LIMONENE, (+)- (UNII: GFD7C86Q1W) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SORBITAN MONOCAPRYLATE (UNII: 1VTA8DCP5Q) MANDARIN OIL (UNII: NJO720F72R) LITSEA OIL (UNII: 2XIW34BN6O) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) PROPANEDIOL (UNII: 5965N8W85T) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49404-153-01 1 in 1 CARTON 12/22/2022 1 50 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49404-153-02 5 mL in 1 TUBE; Type 0: Not a Combination Product 12/22/2022 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 - Have & Be Co., Ltd. (690400408) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co.,LTD. Gwanjeong 2 factory 963271750 manufacture(49404-153)