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Sun wrangler daily mineral sunscreen spf 45 - Medication Information

Product NDC Code 84340-045
Drug Name

Sun wrangler daily mineral sunscreen spf 45

Type Brand
Active Ingredients
Zinc oxide 190 mg/ml
Route TOPICAL
Dosage Form CREAM
Application Number M020
Labeler Name Sun Wrangler
Packages
Package NDC Code Description
84340-045-02 75 ml in 1 tube (84340-045-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Zinc Oxide 19% (Non-Nano)

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. Reapply after 80 minutes of swimming or sweating or immediately after towel drying and at least every 2 hours. For children under 6 months of age; ask a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Deionized Water, Aloe Barbadensis Leaf Juice*, Coco-Caprylate/Caprate, Isoamyl Laurate, Vegetarian Glycerin, Polyglyceryl- 3 Oleate, Propanediol, Polyhydroxystearic Acid, Diisostearoyl Polyglyceryl- 3 Dimer Dinoleate, Mica, Caprylic/Capric Triglyceride, Sodium Chloride, Ethyl lauroyl arginate HCl, Jojoba Esters, Olive Squalane Oil, Extracts of Alaria Esculenta (Wakame Seaweed), Olea Europa (Olive) Leaf*, Camellia Sinenis (Green Tea) Leaf*, Ocimum Tinuiflorum (Tulsi) Leaf*, Cocos Nucifera (Coconut) Oil, Curcuma Longa (Turmeric) Root* Extract, Tetrasodium Glutamate Diacetate, Mixed Tocopherols, Sodium Stearoyl Glutamate, Silica, Xanthan Gum, Calcium Titanium Borosilicate and Titanium.

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.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Sun Wrangler Daily Mineral Sunscreen SPF 45 ZINC OXIDE WATER ALOE VERA LEAF COCO-CAPRYLATE ISOAMYL LAURATE GLYCERIN POLYGLYCERYL-3 OLEATE PROPANEDIOL POLYHYDROXYSTEARIC ACID (2300 MW) DIISOSTEAROYL POLYGLYCERYL-3 DIMER DILINOLEATE MICA TRICAPRIN SODIUM CHLORIDE ETHYL LAUROYL ARGINATE HYDROCHLORIDE HYDROLYZED JOJOBA ESTERS (ACID FORM) OLIVE OIL ALARIA ESCULENTA OLEA EUROPAEA LEAF GREEN TEA LEAF HOLY BASIL LEAF COCONUT OIL TURMERIC TETRASODIUM GLUTAMATE DIACETATE TOCOPHEROL SODIUM STEAROYL GLUTAMATE SILICON DIOXIDE XANTHAN GUM ZINC OXIDE ZINC OXIDE

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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Label

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.
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 this product from excessive heat and sunlight.

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. Stop use and ask a doctor if rash occurs. When using this produc t, keep out of eyes. Rinse with water to remove.

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