Bambusa Pulsatilla Liquid
FDA Label NDC 48951-2014

8 label sections · Submitted to the FDA by Uriel Pharmacy Inc. · 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 Bambusa Pulsatilla (NDC 48951-2014). 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 otc - purpose, indications & usage, dosage & administration, warnings, otc - keep out of reach of children, otc - active ingredient, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

Use: Temporary relief of headache.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Otc - Active Ingredient

Active Ingredients: Viscum Mali (Apple tree mistletoe) 3X, Equisetum (Common horsetail) 5X, Formica (Red wood ant) 5X, Pulsatilla (Pasqueflower) 5X, Bambusa (Bamboo) 6X, Betonica (Wood betony) 6X, Disci interver. (Bovine intervertebral discs of the cervical, thoracic and lumbar spine) 6X, Rosmarinus (Rosemary) 6X, Stannum met. (Metallic tin) 7X, Vivianite (Nat. ferrous phosphate) 7X, Jasper 12X

Inactive Ingredient

Inactive Ingredients: Water, Salt, Lactose

Prepared using rhythmical processes.

Otc - Questions

Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120 shopuriel.com Lot:

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