Be Gone Insomnia
FDA Label NDC 68428-726

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 Insomnia (NDC 68428-726). 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.

Active Ingredients

CHAMOMILLA 6C

COFFEA CRUDA 6C

HYOSCYAMUS 6C

IGNATIA 6C

NUX VOMICA 6C

PASSIFLORA 6C

Uses

Eases insomnia caused by grief, intense mental application and stress. Is a natural sleep aid that is non-habit forming. Will not cause drowsiness and has no side effects.

Keep Out Of Reach Of Children

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

Indications

Indications:

CHAMOMILLA Irritability

COFFEA CRUDA Sleeplessness

HYOSCYAMUS Twitching

IGNATIA Sadness

NUX VOMICA Vomiting

PASSIFLORA Insomnia

Stop Use And Ask Doctor

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

Directions

Adults 2 pellets every 3 hours for 2 days. Then 2 pellets morning and night for 2 weeks.

Children: 1 pellet. Repeat as necessary.

Inactive Ingredients

Sucrose/Lactose

Principal Display Panel

Be gone​TM Insomnia Label

Be goneTM Insomnia Box

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