Zeel

Manufacturer
Biologische Heilmittel Heel
Effective date
2012-02-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:03:34

Label at a glance#

ProductZeel
Active ingredientSILICON DIOXIDE, COMFREY ROOT, ARNICA MONTANA ROOT, TOXICODENDRON PUBESCENS LEAF, SULFUR, SANGUINARIA CANADENSIS ROOT, SOLANUM DULCAMARA STEM, COENZYME A, NADIDE, SODIUM DIETHYL OXALACETATE, .ALPHA.-LIPOIC ACID, SUS SCROFA CARTILAGE, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, SUS SCROFA PLACENTA
Label structure8 sections

Indications and uses

For the temporary relief of: Minor joint pain and stiffness

Dosage and administration

Direction for use: Adults: Apply in the morning and evening to the effected areas, rubbing in gently. If appropriate, also apply an ointment dressing. Children under 18 years of age see a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Each 50g of ointment contains: Silicea 6X 0.5g; Symphytum officinale 8X 0.375g; Arnica montana, radix 2X 0.15g; Rhus toxicodendron 2X 0.135g; Sulphur 6X 0.135g; Sanguinaria canadensis 2X 0.113g; Dulcamara 2X 0.038g; Coenzyme A 6X 0.005g; Nadidum 6X 0.005g; Natrum oxalaceticum 6X 0.005g; α- Lipoicum acidum 6X 0.005g;  Cartilago suis 2X  0.0005g;  Embryo suis 2X  0.0005g;  Funiculus  umbilicalis suis  2X  0.0005g;  Placenta suis  2X  0.0005g.

PURPOSE

OTC - PURPOSE SECTION

Minor joint pain and stiffness

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicine out of the reach of children.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

For the temporary relief of:
  • Minor joint pain and stiffness

WARNINGS

WARNINGS SECTION

Warnings: For external use only. Do not apply to large areas of the body. If symptoms persist or worsen, or if a rash develops a physician should be consulted. In rare cases, allergic skin reactions may develop. Avoid using Zeel in cases of known hypersensitivity to any ingredients in Zeel.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Direction for use: Adults: Apply in the morning and evening to the effected areas, rubbing in gently. If appropriate, also apply an ointment dressing. Children under 18 years of age see a doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients: Cetylstearyl alcohol, ethanol, paraffin, purified water and white petrolatum.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Zeel 50g Carton.jpg
Zeel 50g Carton.jpg

Zeel 50g Carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51885-3353-12019-11-13C16284748780-197449f38-b89a-f6ea-e053-dbdaa90aa7039cd09f43-5049-4aaf-9cae-a017dcb39cf0
51885-3353-32019-11-13C16284748780-197449f38-b89a-f6ea-e053-dbdaa90aa7039cd09f43-5049-4aaf-9cae-a017dcb39cf0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51885-3353-1Zeel1 in 1 CARTONOINTMENT11
51885-3353-1Zeel50 g in 1 TUBEOINTMENT501
51885-3353-3Zeel1 in 1 CARTONOINTMENT11
51885-3353-3Zeel50 g in 1 TUBEOINTMENT501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51885-3353ZEEL (SILICON DIOXIDE AND COMFREY ROOT AND ARNICA MONTANA ROOT AND TOXICODENDRON PUBESCENS LEAF AND SULFUR AND SANGUINARIA CANADENSIS ROOT AND SOLANUM DULCAMARA STEM AND COENZYME A AND NADIDE AND SODIUM DIETHYL OXALACETATE AND .ALPHA.-LIPOIC ACID AND SUS SCROFA CARTILAGE AND SUS SCROFA EMBRYO AND SUS SCROFA UMBILICAL CORD AND SUS SCROFA PLACENTA AND ) OINTMENT [BIOLOGISCHE HEILMITTEL HEEL]1Legacy NDC, 4 package rows20120228_9cd09f43-5049-4aaf-9cae-a017dcb39cf0.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
.ALPHA.-LIPOIC ACIDACTIVE INGREDIENT73Y7P0K73Y1
ARNICA MONTANA ROOTACTIVE INGREDIENTMUE8Y113271
COENZYME AACTIVE INGREDIENTSAA04E81UX1
COMFREY ROOTACTIVE INGREDIENTM9VVZ08EKQ1
NADIDEACTIVE INGREDIENT0U46U6E8UK1
SANGUINARIA CANADENSIS ROOTACTIVE INGREDIENTN9288CD5081
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
SODIUM DIETHYL OXALACETATEACTIVE INGREDIENT6CA025Y4FG1
SOLANUM DULCAMARA STEMACTIVE INGREDIENTIR986LE7DF1
SULFURACTIVE INGREDIENT70FD1KFU701
SUS SCROFA CARTILAGEACTIVE INGREDIENT73ECW5WG2F1
SUS SCROFA EMBRYOACTIVE INGREDIENT9928MC12VO1
SUS SCROFA PLACENTAACTIVE INGREDIENTC8CV8867O81
SUS SCROFA UMBILICAL CORDACTIVE INGREDIENT118OYG6W3H1
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A1
.ALPHA.-LIPOIC ACIDACTIVE MOIETY73Y7P0K73Y1
ARNICA MONTANA ROOTACTIVE MOIETYMUE8Y113271
COENZYME AACTIVE MOIETYSAA04E81UX1
COMFREY ROOTACTIVE MOIETYM9VVZ08EKQ1
NADIDEACTIVE MOIETY0U46U6E8UK1
SANGUINARIA CANADENSIS ROOTACTIVE MOIETYN9288CD5081
SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
SODIUMACTIVE MOIETY9NEZ333N271
SOLANUM DULCAMARA STEMACTIVE MOIETYIR986LE7DF1
SULFURACTIVE MOIETY70FD1KFU701
SUS SCROFA CARTILAGEACTIVE MOIETY73ECW5WG2F1
SUS SCROFA EMBRYOACTIVE MOIETY9928MC12VO1
SUS SCROFA PLACENTAACTIVE MOIETYC8CV8867O81
SUS SCROFA UMBILICAL CORDACTIVE MOIETY118OYG6W3H1
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
CETOSTEARYL ALCOHOLINACTIVE INGREDIENT2DMT128M1S1
PARAFFININACTIVE INGREDIENTI9O0E3H2ZE1
PETROLATUMINACTIVE INGREDIENT4T6H12BN9U1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51885-335351885-3353-1, 51885-3353-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 97 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii candidate
59 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9ULOTION / TOPICAL25 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SOINTMENT / TOPICAL1.2 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / NASAL70 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1STABLET, EXTENDED RELEASE / ORAL800 mgExact identifier — unii candidate
9 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEAEROSOL, FOAM / TOPICAL14235 mgExact identifier — unii candidate
11 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii candidate
59 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCAPSULE, EXTENDED RELEASE / ORAL9.43 mgExact identifier — unii candidate
9 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPASTE / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / SUBCUTANEOUS6.1 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZETABLET / ORAL0.7 mgExact identifier — unii candidate
11 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UTABLET, EXTENDED RELEASE / ORAL0.18 mgExact identifier — unii candidate
18 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZECAPSULE, EXTENDED RELEASE / ORAL100 mgExact identifier — unii candidate
11 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii candidate
59 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / RECTAL38 mgExact identifier — unii candidate
11 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZETABLET, EXTENDED RELEASE / ORAL321 mgExact identifier — unii candidate
11 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SSPRAY / TOPICAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVENOUS99 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVASCULAR100 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVESICAL7892 mgExact identifier — unii candidate
59 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii candidate
18 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT, AUGMENTED / TOPICAL81.94 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAMUSCULAR1000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAVENOUS400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / RECTAL0.35 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAVENOUS6405 mgExact identifier — unii candidate
59 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UCAPSULE, EXTENDED RELEASE / ORAL0.07 mgExact identifier — unii candidate
18 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZETABLET, COATED / ORAL0.07 mgExact identifier — unii candidate
11 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TRANSDERMAL49.37 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UCREAM, AUGMENTED / TOPICAL26 %w/wExact identifier — unii candidate
18 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii candidate
59 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii candidate
11 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / AURICULAR (OTIC)NAExact identifier — unii candidate
18 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MMOUTHWASH / BUCCAL200 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY, METERED / SUBLINGUAL29 mgExact identifier — unii candidate
59 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCREAM / TOPICAL1428 mgExact identifier — unii candidate
9 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAMUSCULAR1491 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAMUSCULAR400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / INTRAVENOUS4000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / DENTAL12.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZETABLET, DELAYED RELEASE / ORAL0.2 mgExact identifier — unii candidate
11 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii candidate
9 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVENOUS92 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZECREAM / TOPICAL300 mgExact identifier — unii candidate
11 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UEMULSION / TOPICAL7.8 %w/wExact identifier — unii candidate
18 equally ranked IID candidates

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
fe3f3fc6-bf04-416d-b1a9-f2a39935608a9cd09f43-5049-4aaf-9cae-a017dcb39cf02012-02-28WarningsExact identifier
spl id: fe3f3fc6-bf04-416d-b1a9-f2a39935608a
spl set id: 9cd09f43-5049-4aaf-9cae-a017dcb39cf0

Reported adverse events (FAERS/openFDA)#

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