Zeel

ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER TOPICAL HUMAN OTC DRUG

Zeel is an FDA drug label for the active ingredient ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER manufactured by Biologische Heilmittel Heel administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230928.

Generic name: ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER
Manufacturer: Biologische Heilmittel Heel
Product type: HUMAN OTC DRUG
Route: TOPICAL
Dosage form: N/A
NDC: 51885-9489
Application: N/A
Label effective: 20230928

About this product

Zeel is an FDA-registered drug product whose active ingredient is ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER. It is labelled by Biologische Heilmittel Heel taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 51885-9489, label effective 20230928. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER are most often described in connection with: indications indications, temporary relief, minor arthritis, joint stuffness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingrendent Active ingredients: Each 100 g contains: _-Lipoicum acidum 6X 0.01g, *Arnica montana, radix 2X 0.3g, *Cartilago suis 2X 0.001g (Final concentration 7X), Coenzyme A 6X 0.01g, *Dulcamara 2X 0.08g, *Embryo suis 2X 0.001g (Final concentration 7X), *Funiculus umbilicalis suis 2X 0.001g (Final concentration 7X) Nadidum 6X 0.01g, Natrum oxalaceticum 6X 0.01g, *Placenta totalis suis 2X 0.001g (Final concentration 7X), *Rhus toxicodendron 2X 0.27g (Final concentration 4X), *Sanguinaria canadensis 2X 0.23g (Final concentration 4X), *Silicea 6X 1g, *Sulphur 6X 0.27g, *Symphytum officinale 8X 0.75g. *Natural Ingredient

Indications & Usage

Indications Indications: For the temporary relief of minor arthritis pain and joint stuffness.

Dosage & Administration

Directions Directions: Adults: Apply generously to affected areas 2 to 3 times daily, or as directed by your health professional. Massage thoroughly into skin. Children under 18 years of age: consult your healthcare professional. Indications: For the temporary relief of minor arthritis pain and joint stiffness

Warnings

Warnings Warnings: For external use only. Do not use if pregnant or breast-feeding. Do not apply over open wounds or broken skin. In rare cases, allergic skin reactions may develop. Keep out of reach of children. If symptoms persist or worsen a healthcare provider should be consulted. If swallowed, get medical help or contact a Poison Control Center right away. Do not use if known sensitivity to Zeel® or any of its ingredients exists.

Frequently asked questions

What is Zeel used for?
Indications Indications: For the temporary relief of minor arthritis pain and joint stuffness.

Who makes Zeel?
Biologische Heilmittel Heel is the labeler of record for Zeel.

What form does Zeel come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Zeel prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Zeel been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.