Cocculus Conium Liquid
FDA Label NDC 48951-3287

9 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 Cocculus Conium (NDC 48951-3287). 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

Indications & Usage

FOR ORAL USE ONLY

Dosage & Administration

Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.

Otc - Active Ingredient

Active Ingredients: Cocculus 4X, Conium (Hemlock) 4X, Ambra grisea (Amber gris) 7X, Petroleum 9X

Inactive Ingredient

Inactive Ingredients: Water, Salt

"prepared using rhythmical processes'

Otc - Purpose

Use: Temporary relief of dizziness.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings:
NOT FOR INJECTION
Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Otc - Questions

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com

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