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Zeel

Heel Inc

Zeel 2.0 ml Injection


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ZEEL DESCRIPTION

 Each 2.0 ml ampule contains:
 Active Ingredients:
 Ingredient name  Potency  Quantity   Final dilution
 a-Lipoicum acidum  8X  2.0 μl  10.99X
 Arnica montana, radix  4X  200.0 μl  5.00X
 Cartilago suis  6X  2.0 μl  9.00X
 Coenzyme A  8X  2.0 μl  10.99X
 Dulcamara  3X  10.0 μl  5.30X
 Embryo totalis suis  6X  2.0 μl  9.00X
 Funiculus umbilicalis suis  6X  2.0 μl  9.00X
 Nadidum  8X  2.0 μl  10.99X
 Natrum oxalaceticum  8X  2.0 μl  10.99X
 Placenta suis  6X  2.0 μl  9.00X
 Rhus toxicodendron  2X  10.0 μl  4.30X
 Sanguinaria canadensis  4X  3.0 μl  6.82X
 Sulphur  6X  3.6 μl  8.74X
 Symphytum officinale  6X  10.0 μl  8.30X

Inactive Ingredients

Water for injection 1,747.4 μl

Sodium Chloride     17.6 μl

ZEEL INDICATIONS AND USAGE

Treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseases

  • Zeel® Injection Solution is a homeopathic drug product indicated for the treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.

Co-administration Therapy with Traumeel® Injection Solution for the treatment of inflammatory and degenerative conditions of the musculoskeletal system.

  • Zeel® Injection Solution is a homeopathic drug product indicated, in combination with Traumeel® Injection Solution, for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.

ZEEL DOSAGE AND ADMINISTRATION

General Considerations

  • The dosage schedules listed below can be used as a general guide for the administration of Zeel® Injection Solution.
  • Zeel® Injection Solution may be administered s.c., i.d., i.m., i.a. or i.v.
  • The interval between injections is left to the discretion of the HCP, but should not exceed 1 ampule in 24 hours.
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Draw up the contents of the ampule into the syringe. Discard half or one third of the contents, depending on the required dosage, before administering.

Standard Dosage - for the treatment of arthrosis/osteoarthritis and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.

Adults and children 12 years and older:

1 ampule 1 to 3 times per 7 days

Children 6 to 11 years:

2/3 of an ampule 1 to 3 times per 7 days

Acute Dosage - for the treatment of arthrosis/osteoarthritis and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.

Adults and children 12 years and older:

1 ampule daily, and then continue with standard dosage

Children 6 to 11 years:

2/3 of an ampule daily, and then continue with standard dosage

Co-administration therapy with Traumeel® Injection Solution - for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.

  • In the treatment of musculoskeletal conditions, if co-administration with another homeopathic medicinal product is desired, Zeel® Injection Solution may be mixed in a ratio of 1:1 with Traumeel® Injection Solution.
  • For convenience, the daily dose of Zeel® Injection Solution may be administered at the same time as a Traumeel® Injection Solution, according to the dosing recommendations for each medication.

ZEEL CONTRAINDICATIONS

  • Zeel® Injection Solution is contraindicated in patients with known hypersensitivity to Zeel® or any of its ingredients.
  • When Zeel® Injection Solution is co-administered with Traumeel® Injection Solution, refer to the Contraindication section of the respective Traumeel® Injection Solution labeling.

WARNINGS AND PRECAUTIONS

Keep out of reach of children.

ZEEL ADVERSE REACTIONS

Post Marketing Experience

  • The following adverse events have been identified during post-marketing use of Zeel® Injection Solution. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frquency or establish a causal relationship to drug exposure.

  • Adverse event rates observed in Monotherapy use of Zeel® Injection Solution: Allergic (hypersensitivity) skin reactions may occur in isolated cases.

  • Adverse event rates observed in the Monotherapy use of Traumeel® Injection Solution: Allergic (hypersensitivity) reactions (e.g. skin allergies, redness/swelling at the injection site, even up to anaphylaxis) may occur in isolated cases.

To report SUSPECTED ADVERSE REACTIONS, contact Heel Inc. at 1.800.920.9203

info@heelusa.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

OVERDOSAGE

No negative effects of an overdose have been reported and none are expected due to the homeopathic dilutions.

CLINICAL PHARMACOLOGY

Mechanism of Action

The exact mechanism of Zeel® Injection Solution is not fully understood.

Pharmacodynamics

Not applicable for homeopathic medicinal products.

DOSAGE

One ampule containing 2.0 ml each containing the active ingredients in the strengths listed under Description.

Zeel

Zeel

ARNICA MONTANA ROOT, TOXICODENDRON PUBESCENS LEAF, SOLANUM DULCAMARA TOP, COMFREY ROOT, SULFUR, SANGUINARIA CANADENSIS ROOT, SUS SCROFA CARTILAGE, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, SUS SCROFA PLACENTA, .ALPHA.-LIPOIC ACID, COENZYME A, NADIDE and SODIUM DIETHYL OXALACETATE INJECTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:50114-7030
Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARNICA MONTANA ROOT ARNICA MONTANA ROOT 4 [hp_X]
TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF 2 [hp_X]
Solanum Dulcamara Top Solanum Dulcamara Top 3 [hp_X]
COMFREY ROOT COMFREY ROOT 6 [hp_X]
SULFUR SULFUR 6 [hp_X]
SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT 4 [hp_X]
SUS SCROFA CARTILAGE Sus Scrofa Cartilage 6 [hp_X]
SUS SCROFA EMBRYO SUS SCROFA EMBRYO 6 [hp_X]
SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD 6 [hp_X]
SUS SCROFA PLACENTA SUS SCROFA PLACENTA 6 [hp_X]
.ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID 8 [hp_X]
COENZYME A COENZYME A 8 [hp_X]
NADIDE NADIDE 8 [hp_X]
SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE 8 [hp_X]

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 2.0 in 1 AMPULE
2 2.0 in 1 AMPULE
3 NDC:50114-7030-2 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2004-01-31


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