Zeel
FDA Label NDC 62795-9494

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 Zeel (NDC 62795-9494). 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:, warnings:, directions:, inactive ingredients:, keep out of reach of children, purpose, active ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Indications:

For the temporary relief of minor arthitis
pain, joint pain and stiffness.

Warnings:

 If pregnant or breast-feeding, ask a
health professional before use. Keep out of reach of
children. If symptoms persist or worsen, a healthcare
provider should be consulted. Do not use if known
sensitivity to Zeel® or any of its ingredients exists.

Directions:

Adults: 1-2 tablets 3 times per day or
as directed by a health practitioner. Not to exceed
6 tablets per 24 hours. Children under 18,
as directed by a health professional. Allow to
completely dissolve in the mouth.

Inactive Ingredients:

 Lactose, Magnesium stearate

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Purpose

Arthritis Pain
Relief

Active Ingredients:

Each 300 mg tablet contains:
Alpha Lipoicum acidum 6X 0.03mg, *Arnica
montana, radix 1X 0.6mg, *Cartilago suis 4X 0.3mg,
Coenzyme A 6X 0.03mg, *Dulcamara 2X 0.15mg,
*Embryo suis 4X 30mg, *Funiculus umbilicalis suis 4X
30mg, Nadidum 6X 0.03mg, Natrum oxalaceticum
6X 0.03mg, *Placenta totalis suis 4X 0.3mg, *Rhus
tox 2X 0.54mg, *Sanguinaria canadensis 3X 0.45mg,
*Silicea 6X 3mg, *Sulphur 6X 0.54mg, *Symphytum
officinale 8X 0.15mg. *Natural

* Please review the disclaimer below.