Label: 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

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated September 28, 2023

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  • 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

    Zeel.jpg

  • 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:62795-9494
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y) (.ALPHA.-LIPOIC ACID - UNII:73Y7P0K73Y) ALPHA LIPOIC ACID6 [hp_X]
    ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT1 [hp_X]
    SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F) SUS SCROFA CARTILAGE4 [hp_X]
    COENZYME A (UNII: SAA04E81UX) (COENZYME A - UNII:SAA04E81UX) COENZYME A6 [hp_X]
    SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP2 [hp_X]
    SUS SCROFA EMBRYO (UNII: 9928MC12VO) (SUS SCROFA EMBRYO - UNII:9928MC12VO) SUS SCROFA EMBRYO4 [hp_X]
    SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (SUS SCROFA UMBILICAL CORD - UNII:118OYG6W3H) SUS SCROFA UMBILICAL CORD4 [hp_X]
    NADIDE (UNII: 0U46U6E8UK) (NADIDE - UNII:0U46U6E8UK) NADIDE6 [hp_X]
    SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (DIETHYL OXALACETATE - UNII:15S56468G7) SODIUM DIETHYL OXALACETATE6 [hp_X]
    SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8) SUS SCROFA PLACENTA4 [hp_X]
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF2 [hp_X]
    SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508) SANGUINARIA CANADENSIS ROOT3 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 [hp_X]
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR6 [hp_X]
    COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT8 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code H
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62795-9494-21 in 1 CARTON01/12/2022
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/12/2022
    Labeler - MediNatura Inc (079324099)
    Establishment
    NameAddressID/FEIBusiness Operations
    Biologische Heilmittel Heel315635359manufacture(62795-9494)
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