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Omnilux mineral facial sunscreen - Medication Information

Product NDC Code 83866-6202
Drug Name

Omnilux mineral facial sunscreen

Type Brand
Active Ingredients
Zinc oxide 132 mg/ml
Route TOPICAL
Dosage Form LOTION
Application Number M020
Labeler Name The Lotus Global Group, Inc, dba GlobalMed Technologies
Packages
Package NDC Code Description
83866-6202-2 1 bottle, pump in 1 carton (83866-6202-2) / 50 ml in 1 bottle, pump (83866-6202-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Omnilux Mineral Facial Sunscreen Active Ingredients

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.
Omnilux Mineral Facial Sunscreen Dosage and Administration

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Omnilux Mineral Facial Sunscreen Inactive ingredients

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.
Omnilux Mineral Facial Sunscreen Indications & usage

Purpose

Information about the drug product’s indications for use.
Omnilux Mineral Facial Sunscreen purpose

Spl product data elements

Usually a list of ingredients in a drug product.
Omnilux Mineral Facial Sunscreen Zinc Oxide ALLANTOIN SODIUM HYDROXIDE LECITHIN, SOYBEAN POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE HYDROLYZED JOJOBA ESTERS (ACID FORM) METHYLPROPANEDIOL CAPRYLYL GLYCOL PHENYLPROPANOL XANTHAN GUM ISOAMYL LAURATE HEXYLENE GLYCOL TOCOPHEROL CETYL ALCOHOL ETHYLHEXYLGLYCERIN GLYCERIN SILICON DIOXIDE WATER .ALPHA.-BISABOLOL, (+)- BUTYLOCTYL SALICYLATE CETETH-20 PULLULAN SQUALANE STEARETH-20 ZINC OXIDE ZINC OXIDE ALOE VERA LEAF FERRIC OXIDE YELLOW PEG-75 STEARATE TETRASODIUM GLUTAMATE DIACETATE POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE PHENOXYETHANOL RUTIN

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.
Omnilux Mineral Facial Sunscreen PDP

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.
Omnilux Mineral Facial Sunscreen keep out of reach of children

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.
Omnilux Mineral Facial Sunscreen Warning Label

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