Purpose
Uses: For temporary relief of fatigue and stiffness, kidney support.
Birch Juniper Rejuvenation
FDA Label NDC 48951-2071
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 Birch Juniper Rejuvenation (NDC 48951-2071). 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 purpose, dosage & administration, otc-active ingredient, inactive ingredient, keep out of reach of children, do not use section, ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Directions: Ages 12 and older: Take 1-2 teaspoons by mouth morning and evening, undiluted or with water. Under age 12: Ask a doctor.
SHAKE WELL BEFORE USE. REFRIGERATE AFTER OPENING.
Otc-Active Ingredient
Active Ingredients: Extract of Betula e fol. 1X HPUS, Juniperus e fruct. 1X HPUS.
Inactive Ingredient
Inactive Ingredients: Water, Organic cane sugar, Honey, Citric acid.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Do Not Use Section
Warnings:
Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.
Ask Doctor Section
Consult a doctor if symptoms persist or worsen.
Pregnancy Or Breast Feeding Section
If you are pregnant or nursing, consult a doctor before use.
Questions Section
Made with care byUriel PharmacyEast Troy, WI 53120Questions or comments?Please call 1.866.642.2858www.urielpharmacy.comNDC 48951-2071-9
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Birch Juniper
Rejuvenation Syrup
Homeopathic
net vol. 260 ml (8.8 fl. oz.)
Birch Juniper Syrup Bottle Label (Birjuns01)
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