Dosage and administration
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.
Zeel
- Manufacturer
- MediNatura Inc | Biologische Heilmittel Heel
- Effective date
- 2023-09-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:22:23
Label at a glance#
ProductZeel
Active ingredientALPHA LIPOIC ACID, ARNICA MONTANA ROOT, 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, COMFREY ROOT
Label structure8 sections
Label contents#
Full prescribing information#
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
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62795-9494-2 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-b033-d83d-e063-dadaa90ab31f | Zeel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62795-9494-2 | Zeel | 100 in 1 BOTTLE | TABLET | 100 | 2 | |
| 62795-9494-2 | Zeel | 1 in 1 CARTON | TABLET | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62795-9494 | ZEEL (ALPHA LIPOIC ACID, ARNICA MONTANAROOT,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,COMFREY ROOT) TABLET [MEDINATURA INC] | 2 | Legacy NDC, 2 package rows | 20230929_7d22f888-88fa-4ebc-9c29-edf1e3514f4d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 62795-9494-2 | EA - Each | 62795-9494 | af593c98-a98c-484d-96e3-c33b7b8a8141 | 1 | 2022-05-04 |
Products#
Every source-derived product name is available through these pages.
- Zeel
- ALPHA LIPOIC ACID, ARNICA MONTANAROOT,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,COMFREY ROOT
- ALPHA LIPOIC ACID
- .ALPHA.-LIPOIC ACID
- ARNICA MONTANA ROOT
- SUS SCROFA CARTILAGE
- COENZYME A
- SOLANUM DULCAMARA TOP
- SUS SCROFA EMBRYO
- SUS SCROFA UMBILICAL CORD
- NADIDE
- SODIUM DIETHYL OXALACETATE
- DIETHYL OXALACETATE
- SUS SCROFA PLACENTA
- TOXICODENDRON PUBESCENS LEAF
- SANGUINARIA CANADENSIS ROOT
- SILICON DIOXIDE
- SULFUR
- COMFREY ROOT
- LACTOSE, UNSPECIFIED FORM
- MAGNESIUM STEARATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62795-9494 | 62795-9494-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 00923ff7-9639-44eb-829a-92f238ec9eb4 | 7d22f888-88fa-4ebc-9c29-edf1e3514f4d | 2023-09-28 | Warnings | 00923ff7-9639-44eb-829a-92f238ec9eb4 7d22f888-88fa-4ebc-9c29-edf1e3514f4d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.