Hay Fever
FDA Label NDC 64117-176

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Natural Health Supply for the product Hay Fever (NDC 64117-176). 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, active ingredient, directions, keep out of reach of children, warning, inactive ingredients, purpose, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Indications

Indications: To be used for acute self-limiting conditions according to standard homeopathic indications

Active Ingredient

SABADILLA

Directions

Take at onset of symptoms.  Repeat every 2 hours or as needed until relieved.  If condition persists or worsens discontinue use and consult a practitioner.

Adults: dissolve 5-10 pellets in 1 oz. of filtered water or take dry by mouth.  Children and infants: 1-5 pellets.

Keep Out Of Reach Of Children

Keep these and all medications out of the reach of children.

Warning

If pregnant or nursing, consult a practitioner before using.

Inactive Ingredients

Inactive Ingredients - Lactose, Sucrose

Purpose

Purpose: Hay Fever

Package Label

Est. No. 1724217

Natural Health Supply

505-474-9175

Homeopathic Medicated Pellets

Do not use if clear bottle seal is broken

SABADILLA 30C

Hay Fever




Lot #__________________

Hay Fever Label (Nhs Hay Fever)

Hay Fever Label (Nhs Hay Fever)

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