Indications & Usage
Directions: FOR ORAL USE.
Aquilinum Taraxicum
FDA Label NDC 48951-1067
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Aquilinum Taraxicum (NDC 48951-1067). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Take the contents of one ampule
under the tongue and hold for
30 seconds, then swallow.
Otc - Active Ingredient
Active Ingredients: Chelidonium (Greater celandine) 5X, Filix (Male fern) 5X, Pteridium (Eagle fern) 5X, Salix purpurea (Purple willow) 5X, Salix vitellina (Golden willow) 5X, Salix viminalis (Osier willow) 5X, Scolopendrium (Hart’s tongue) 5X, Solidago (Goldenrod) 5X, Taraxacum (Dandelion) 5X
Inactive Ingredient
Inactive Ingredients: Water, Salt
Otc - Purpose
Use: Temporary relief of digestive upset.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions
worsen or persist. If pregnant or nursing, consult a doctor before use. Natural ingredients may cause color, scent
and/or taste variation.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
Package Label.Principal Display Panel
Aquilinumtaraxcumampule (Aquilinumtaraxacumampule)
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