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Sunsolve md correct and fade - Medication Information

Product NDC Code 84878-200
Drug Name

Sunsolve md correct and fade

Type Brand
Active Ingredients
Zinc oxide 132 mg/ml
Route TOPICAL
Dosage Form LOTION
Application Number M020
Labeler Name Sunsolve MD Inc
Packages
Package NDC Code Description
84878-200-02 1 bottle, pump in 1 carton (84878-200-02) / 48 ml in 1 bottle, pump (84878-200-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Sunsolve MD Correct and Fade 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.
Sunsolve MD Correct and Fade Dosage and Administration

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Sunsolve MD Correct and Fade 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.
Sunsolve MD Correct and Fade Indications & usage

Purpose

Information about the drug product’s indications for use.
Sunsolve MD Correct and Fade Sunsolve MD Correct and Fade purpose

Spl product data elements

Usually a list of ingredients in a drug product.
Sunsolve MD Correct and Fade Zinc Oxide FERROSOFERRIC OXIDE FERRIC OXIDE YELLOW PHENOXYETHANOL CAPRYLIC/CAPRIC TRIGLYCERIDE FERRIC OXIDE RED GLYCERIN TOCOPHEROL GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT JOJOBA OIL ORYZA SATIVA WHOLE TRIDECYL SALICYLATE SILICON DIOXIDE CAPRYLYL GLYCOL COCO-CAPRYLATE NYLON-12 PHENYLPROPANOL HELIANTHUS ANNUUS FLOWERING TOP LECITHIN, SOYBEAN METHYLPROPANEDIOL POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE ALLANTOIN ZINC OXIDE ZINC OXIDE ALKYL (C12-15) BENZOATE ROSMARINUS OFFICINALIS FLOWER .ALPHA.-BISABOLOL, (+)- SODIUM HYDROXIDE WATER NIACINAMIDE PROPANEDIOL TETRASODIUM GLUTAMATE DIACETATE SODIUM CHLORIDE POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE STEARALKONIUM HECTORITE POLYGLYCERYL-3 DIISOSTEARATE

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.
Sunsolve MD Correct and Fade 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.
Sunsolve MD Correct and Fade 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.
Sunsolve MD Correct and Fade 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