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Salyntra - Medication Information

Product NDC Code 83592-125
Drug Name

Salyntra

Type Brand
Active Ingredients
Salicylic acid 6 g/100g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 312893,
2672367
Labeler Name True Marker Pharmaceuticals, Inc.
Packages
Package NDC Code Description
83592-125-60 60 g in 1 bottle, plastic (83592-125-60)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient salicylic acid 6%

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.
Directions Apply SALYNTRA GEL thoroughly to the affected area and occlude the area at night. Preferably, the skin should be hydrated (soaked in water) for at lest five minutes prior to application. The medication is washed off in the morning. In those areas where occlusion is difficult or impossible, application is washed off in the morning. In those areas where occlusion is difficult or impossible, application may be made more frequently. Once clearing is apparent, the occasional use of SALYNTRA GEL will usually maintain the remission. Unless hands are being treated, hands should be rinsed thoroughly after application.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients hydroxypropyl cellulose, propylene glycol

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.
Uses For the removal of excess keratin in hyperkeratotic disorders, including scaling associated with psoriasis or thickened skin of palms and soles, corns and calluses.

Spl product data elements

Usually a list of ingredients in a drug product.
SALYNTRA SALICYLIC ACID HYDROXYPROPYL CELLULOSE, UNSPECIFIED PROPYLENE GLYCOL SALICYLIC ACID SALICYLIC ACID

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.
Product label image description image description image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other Information Store at controlled room temperature 59 to 86 F (15 to 30 C) Questions or comments? call 877-887-9879

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.
Warnings For external use only. Avoid contact with eyes an other mucous membranes. May cause mild irritation. If excessive irritation or sensitivity occurs, discontinue use and consult with your physician. Do not use on children under 2 years of age . Read package insert carefully. Flammable. Keep away from heat and open flame. Keep this and all medications out of reach of children.

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