Be Gone Poison Ivy
FDA Label NDC 68428-725

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Washington Homeopathic Products for the product Be Gone Poison Ivy (NDC 68428-725). 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 active ingredients, uses, keep out of reach of children, indications, stop use and ask doctor, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

RHUS TOX 4X

Uses

To relieve the symptoms of conditions produced by Poison Oak and Poison Ivy

Keep Out Of Reach Of Children

As with all medications, keep out of reach of children.

Indications

Indications:

RHUS TOX   Better motion

Stop Use And Ask Doctor

If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.

Directions

Adults 2 pills. Children: 1 pellet. Disolve on tongue every two hours for four doses. Then every three or four hours. Take at greater intervals as condition subsides.

Inactive Ingredients

Sucrose/Lactose

Principal Display Panel

Be gone​TM Poison Ivy label

Be goneTM Poison Ivy box

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