Indications & Usage
Directions: FOR ORAL USE ONLY.
Berberis Oxalis Special Order
FDA Label NDC 48951-2139
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 Oxalis Special Order (NDC 48951-2139). 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 - keep out of reach of children, warnings, otc - questions, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.
Otc - Active Ingredient
Active Ingredients: Berberis e pl. tota 2X, Oxalis e pl. tota 3X, Sabal serr. e fruct. 3X, Urtica urens ex herba 3X, Viscum Abietis e pl. tota 4X, Magnesium sulf. 6X, Prostata 8X, Granite 10X
Inactive Ingredient
Inactive Ingredients: Distilled water, 20% Organic cane alcohol
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. Do not use if safety seal is broken or missing.
Otc - Questions
Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com
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