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Product NDC Code | 24909-063 | ||||||||
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Drug Name | Terrasil ipl relief |
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Type | Brand | ||||||||
Active Ingredients |
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Route | TOPICAL | ||||||||
Dosage Form | OINTMENT | ||||||||
Labeler Name | Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions | ||||||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Purpose Graphite 10X HPUS .................................................... Itching lesion relief Natrum Muriaticum 3X HPUS .................................. Itching & burning relief Symphytum Officinale (Comfrey) 1X HPUS .............Inflammatory relief Thuja Occidentalis 3X HPUS..................................... Papule and naevi symptom relief The letters HPUS indicate the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.
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 Wash and dry affected skin. Apply a layer of ointment 2 to 3 times daily.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients beeswax, coconut oil (organic), cottonseed oil, eucalyptus oil, jojoba oil, lemongrass oil, lysine, magnesium oxide, MCT oil, peppermint oil, silver stearate, zinc oxide
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 Relief from symptoms of: • papules (bumps) • itchy lesions
Spl product data elements
Usually a list of ingredients in a drug product.terrasil IPL Relief GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG YELLOW WAX COCONUT OIL COTTONSEED OIL EUCALYPTUS OIL JOJOBA OIL WEST INDIAN LEMONGRASS OIL LYSINE MAGNESIUM OXIDE PALM OIL PEPPERMINT OIL SILVER STEARATE ZINC OXIDE GRAPHITE GRAPHITE SODIUM CHLORIDE CHLORIDE ION SYMPHYTUM OFFICINALE WHOLE SYMPHYTUM OFFICINALE WHOLE THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG
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
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 room temperature. May temporarily (washable) discolor skin and fabrics in 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.Warnings For external use only . Virally based infections are contagious. This product will not stop the spread of viruses. Do not use • in the eyes • over large areas of the body • if you are allergic to any ingredients in this product. Ask a doctor before use if pregnant or nursing. Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days. Keep out of reach of children. If swallowed, call Poison Control or seek medical help.
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