Mucus Relief Tablet
FDA Label NDC 62795-1012

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medinatura Inc for the product Mucus Relief (NDC 62795-1012). 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 questions?, active ingredient, inactive ingredient, purpose, uses:, directions, keep out of reach of children, bhi mucus relief, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Questions?

Call weekdays: 9am - 5pm EDT 1-844-MediNatura (1-844-633-4628) or email [email protected]

Active Ingredient

Each tablet contains:

Antimonium tartaricum 5X, *Belladonna 6X, *Bryonia alba 6X, *Hepatica triloba 6X, *Hyoscyamus niger 5X, *Ipecacuanha 6X, *Lobelia inflata 4X, *Pertussinum 30X, *Sticta pulmonaria 5X 33.3 mg each.

*Natural Ingredients

Inactive Ingredient

Lactose, Magnesium stearate

Purpose

Mucus Relief Tablets

Relieves:

• Chest Congestion

• Mucus Build-up

• Cough

Uses:

For the temporary relief of minor chest congestion and cough due to mucus build-up

Directions

At first sign of symptoms:

Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 12 tablets in 24 hours.

Standard dosage: Adults and children 4 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours.

For children under 4, consult your health professional.

Allow tablets to dissolve completely in the mouth, do not swallow.

Keep Out Of Reach Of Children

Keep out of reach of children.

* Please review the disclaimer below.