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

Zeel by

Drug Labeling and Warnings

Zeel by is a Homeopathic medication manufactured, distributed, or labeled by MediNatura Inc, Biologische Heilmittel Heel. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62795-9494
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y) (.ALPHA.-LIPOIC ACID - UNII:73Y7P0K73Y)	ALPHA LIPOIC ACID	6 [hp_X]
ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327)	ARNICA MONTANA ROOT	1 [hp_X]
SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F)	SUS SCROFA CARTILAGE	4 [hp_X]
COENZYME A (UNII: SAA04E81UX) (COENZYME A - UNII:SAA04E81UX)	COENZYME A	6 [hp_X]
SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N)	SOLANUM DULCAMARA TOP	2 [hp_X]
SUS SCROFA EMBRYO (UNII: 9928MC12VO) (SUS SCROFA EMBRYO - UNII:9928MC12VO)	SUS SCROFA EMBRYO	4 [hp_X]
SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (SUS SCROFA UMBILICAL CORD - UNII:118OYG6W3H)	SUS SCROFA UMBILICAL CORD	4 [hp_X]
NADIDE (UNII: 0U46U6E8UK) (NADIDE - UNII:0U46U6E8UK)	NADIDE	6 [hp_X]
SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (DIETHYL OXALACETATE - UNII:15S56468G7)	SODIUM DIETHYL OXALACETATE	6 [hp_X]
SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8)	SUS SCROFA PLACENTA	4 [hp_X]
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	2 [hp_X]
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	3 [hp_X]
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	6 [hp_X]
COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ)	COMFREY ROOT	8 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	H
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62795-9494-2	1 in 1 CARTON	01/12/2022
1		100 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/12/2022

Labeler - MediNatura Inc (079324099)

Establishment
Name	Address	ID/FEI	Business Operations
Biologische Heilmittel Heel		315635359	manufacture(62795-9494)