Indications & Usage
Directions: FOR RECTAL USE.
Berberis Populus Adult Size
FDA Label NDC 48951-2146
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 Berberis Populus Adult Size (NDC 48951-2146). 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
Insert 1 suppository as needed.
Otc - Active Ingredient
Active Ingredients: Berberis (Barberry) 3X, Populus trem. (Aspen) 3X, Sabal serr. (Dwarf palm) 3X, Urtica urens (Small nettle) 3X, Resina laricis (Larch resin) 8X, Piper nig. (Black pepper) 17X
Inactive Ingredient
Inactive Ingredients: Cocoa butter, Hydrogenated vegetable oil, Micronized silica gel
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
KEEP REFRIGERATED OR STORE IN COOL, DRY PLACE. REFRIGERATE TO RESOLIDIFY.
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. 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. Do not use if safety seals on box are broken or missing.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com
Package Label.Principal Display Panel
Berberispopadultsupp (Berberispopulusadultsuppository)
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