Zeel Ointment

Manufacturer
Biologische Heilmittel Heel
Effective date
2023-09-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:22:24

Label at a glance#

ProductZeel
Active ingredientALPHA 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
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Warnings

WARNINGS SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Cetostearyl alcohol, Paraffin, Ethanol, Puriffied water, White Petrolatum 

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Indications

INDICATIONS & USAGE SECTION

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

Purpose

OTC - PURPOSE SECTION

Arthritis Pain Relief

Active Ingrendent

OTC - ACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Zeel Ointment.jpgZeel Ointment.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51885-9489-8Zeel1 in 1 CARTONOINTMENT13
51885-9489-8Zeel100 g in 1 TUBEOINTMENT1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51885-9489ZEEL (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) OINTMENT [BIOLOGISCHE HEILMITTEL HEEL]3Current NDC, Legacy NDC, 2 package rows20230929_d5d7a2e5-a6ce-4a41-9430-1378023aa7d0.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51885-948951885-9489-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZeelALPHA 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,CORIANDERBiologische Heilmittel Heeld5d7a2e5-a6ce-4a41-9430-1378023aa7d02023-09-28WarningsExact identifier
ndc (package): 51885-9489-8
ndc (product): 51885-9489
ndc11 (package): 51885948908
spl id: 49ef1c5d-a07b-4bc0-9de1-dc40d8477d8f
spl set id: d5d7a2e5-a6ce-4a41-9430-1378023aa7d0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.