Bryonia Alba
FDA Label NDC 57471-3061

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Celletech Ltd. for the product Bryonia Alba (NDC 57471-3061). 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 warning, keep out of reach of children, maximum dose, active ingredient, inactive ingredient, usage, purpose, manufacturer info, etc., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Warning

WARNING: DO NOT USE IF PLASTIC OUTER SEAL AROUND CAP BROKEN OR MISSING.

IF SYMPTOMS WORSEN OR PERSIST OR IF PREGNANT OR NURSING, SEEK ADVICE OF A DOCTOR

Keep Out Of Reach Of Children

KEEP ALL MEDICINES OUT OF THE REACH OF CHILDREN.

Maximum Dose

MAXIMUM DOSE:

ADULT: 4 pellets, 4 times a day or less.

CHILDREN: 1/2 of adult dose

Active Ingredient

Bryonia Alba 30C

Inactive Ingredient

NON LACTOSE PELLETS:

70% sucrose, 30% starch of corn.

Usage

USES: PER STANDARD HOMEOPATHIC INDICATIONS.

Purpose

USES: PER STANDARD HOMEOPATHIC INDICATIONS.

Manufacturer Info, Etc.

CONTAINS NO LACTOSE OR ANIMAL PRODUCTS

MADE IN THE U.S.A.

NDC #57471

1-800-607-7447 KENT and ALLEN MADISON, WI 53714

Kosher

KOSHER PARVE #1992

Traditional Homeopathic Medicine

TRADITIONAL HOMEOPATHIC MEDICINE (Generation #1)

Principal Display Panel

BRYONIA ALBA

30C

800 PELLETS

HOM 073

Image Of Bottle Label (Bryoniaalba30c)

Image Of Bottle Label (Bryoniaalba30c)

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