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Zeel (Biologische Heilmittel Heel)

Available Formats

Dosage Form Package Information Links
OINTMENT 1 TUBE in 1 CARTON (51885-3353-3) > 50 g in 1 TUBE Label Information
OINTMENT 1 TUBE in 1 CARTON (51885-3353-1) > 50 g in 1 TUBE Label Information

Complete Zeel Information

  • ACTIVE INGREDIENTS

    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

    Minor joint pain and stiffness


  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicine out of the reach of children.
  • INDICATIONS AND USAGE

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

  • WARNINGS

    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

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

  • PRINCIPAL DISPLAY PANEL

    Zeel 50g Carton.jpg

    Zeel 50g Carton.jpg

  • INGREDIENTS AND APPEARANCE
    ZEEL 
    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
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51885-3353
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_X]  in 50 g
    COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 8 [hp_X]  in 50 g
    ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT 2 [hp_X]  in 50 g
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 2 [hp_X]  in 50 g
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_X]  in 50 g
    SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508) SANGUINARIA CANADENSIS ROOT 2 [hp_X]  in 50 g
    SOLANUM DULCAMARA STEM (UNII: IR986LE7DF) (SOLANUM DULCAMARA STEM - UNII:IR986LE7DF) SOLANUM DULCAMARA STEM 2 [hp_X]  in 50 g
    COENZYME A (UNII: SAA04E81UX) (COENZYME A - UNII:SAA04E81UX) COENZYME A 6 [hp_X]  in 50 g
    NADIDE (UNII: 0U46U6E8UK) (NADIDE - UNII:0U46U6E8UK) NADIDE 6 [hp_X]  in 50 g
    SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (SODIUM - UNII:9NEZ333N27) SODIUM DIETHYL OXALACETATE 6 [hp_X]  in 50 g
    .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (.ALPHA.-LIPOIC ACID - UNII:73Y7P0K73Y) .ALPHA.-LIPOIC ACID 6 [hp_X]  in 50 g
    SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F) SUS SCROFA CARTILAGE 2 [hp_X]  in 50 g
    SUS SCROFA EMBRYO (UNII: 9928MC12VO) (SUS SCROFA EMBRYO - UNII:9928MC12VO) SUS SCROFA EMBRYO 2 [hp_X]  in 50 g
    SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (SUS SCROFA UMBILICAL CORD - UNII:118OYG6W3H) SUS SCROFA UMBILICAL CORD 2 [hp_X]  in 50 g
    SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8) SUS SCROFA PLACENTA 2 [hp_X]  in 50 g
    Inactive Ingredients
    Ingredient Name Strength
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51885-3353-1 1 in 1 CARTON
    1 50 g in 1 TUBE
    2 NDC:51885-3353-3 1 in 1 CARTON
    2 50 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 10/20/2011
    Labeler - Biologische Heilmittel Heel (315635359)