Sign In

Save up to 80% by drug discount in your pharmacy with "Pharmacy Near Me - National Drug Discount Card"

You can scan QR Code(just open camera on your phone/scan by application) from the image on prescription drug discount card to save it to your mobile phone. Or just click on image if you're on mobile phone.

View Generic:
View Brand:

Dr.jart every sun day mineral sun screen - Medication Information

Product NDC Code 49404-143
Drug Name

Dr.jart every sun day mineral sun screen

Type Brand
Pharm Class Copper Absorption Inhibitor [EPC],
Decreased Copper Ion Absorption [PE]
Active Ingredients
Titanium dioxide 2.05 mg/50ml
Zinc oxide 5.75 mg/50ml
Route TOPICAL
Dosage Form CREAM
Application Number M020
Labeler Name Have & Be Co., Ltd.
Packages
Package NDC Code Description
49404-143-02 1 container in 1 carton (49404-143-02) / 50 ml in 1 container
49404-143-03 5 ml in 1 tube (49404-143-03)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Zinc Oxide 11.5% Titanium Dioxide 4.1%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Water, CYCLOPENTASILOXANE, PROPANEDIOL, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, LAURYL POLYGLYCERYL-3POLYDIMETHYLSILOXYETHYL DIMETHICONE, METHYL METHACRYLATE CROSSPOLYMER, BUTYLOCTYL SALICYLATE, CAPRYLYL METHICONE, 1,2-HEXANEDIOL, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, STEARIC ACID, ALUMINUM HYDROXIDE, POLYGLYCERYL-3, POLYDIMETHYLSILOXYETHYLDIMETHICONE, TRIETHOXYCAPRYLYLSILANE, SORBITAN CAPRYLATE, CITRUS AURANTIUM DULCIS (ORANGE) OIL, GLYCERYL CAPRYLATE, ETHYLHEXYLGLYCERIN, CITRUS NOBILIS (MANDARIN ORANGE) PEEL OIL, LITSEA CUBEBA FRUIT OIL, TOCOPHEROL

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Helps prevent sunburn If used as directed with other sun protection meausres (see Directions ), decreases the risk of skin cancer and early skin aging casued by the sun

Purpose

Information about the drug product’s indications for use.
Sunscreen

Spl product data elements

Usually a list of ingredients in a drug product.
Dr.Jart Every Sun Day Mineral Sun Screen Zinc Oxide, Titanium Dioxide WATER CYCLOMETHICONE 5 PROPANEDIOL BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER BUTYLOCTYL SALICYLATE CAPRYLYL TRISILOXANE 1,2-HEXANEDIOL DISTEARDIMONIUM HECTORITE MAGNESIUM SULFATE, UNSPECIFIED FORM STEARIC ACID ALUMINUM HYDROXIDE POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) TITANIUM DIOXIDE TITANIUM DIOXIDE ZINC OXIDE ZINC CATION

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
image description

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Protect the product in this container from excessive heat and direct sunlight You may report a serious adverse event from use of this product to: Report Reaction, LLC PO Box 22 Plainsboro, NJ 08536-0222

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 using and ask a doctor if rash occurs.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API