Hay Fever
FDA Label NDC 68428-011

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 Hay Fever (NDC 68428-011). 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

ALLIUM CEPA    6C

ANTHOXANTHUM    6C

SABADILLA       6C

Uses

To relieve the symptoms of itching of the roof of the mouth, watery discharge from the eyes and nose, loss of smell and taste, difficulty breathing. Seasonal Allergies.

Keep Out Of Reach Of Children

Keep this and all medicines out of reach of children.

Indications

Indications:

ALLIUM CEPA    Head cold

ANTHOXANTHUM    Hay fever

SABADILLA      Hay fever

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

Image Of Bottle Label (Hayfever)

Image Of Bottle Label (Hayfever)

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