Label: ZEEL- alpha lipoic acid, arnica montana whole,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,coriander ointment

  • NDC Code(s): 51885-9489-8
  • Packager: Biologische Heilmittel Heel
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

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 August 25, 2022

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  • Warnings

    Warnings: For external use only. Do not use if
    pregnant or breast-feeding. Do not apply over open
    wounds or broken skin. In rare cases, allergic skin reactions
    may develop. Keep out of reach of children. If
    symptoms persist or worsen a healthcare provider should be
    consulted. If swallowed, get medical help or contact a
    Poison Control Center right away. Do not use if known
    sensitivity to Zeel® or any of its ingredients exists.

  • Directions

    Directions: Adults: Apply generously to affected areas
    2 to 3 times daily, or as directed by your health professional.
    Massage thoroughly into skin. Children under 18 years
    of age: consult your healthcare professional.
    Indications: For the temporary relief of minor arthritis
    pain and joint stiffness

  • Inactive ingredients:

    Inactive ingredients:
    Cetostearyl alcohol, Paraffin, Ethanol, Puriffied water, White Petrolatum 

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Indications

    Indications: For the temporary relief of minor arthritis pain and joint stuffness.

  • Purpose

    Arthritis Pain Relief

  • Active Ingrendent

    Active ingredients: Each 100 g contains: _-Lipoicum acidum
    6X 0.01g, *Arnica montana, radix 2X 0.3g, *Cartilago suis 2X
    0.001g (Final concentration 7X), Coenzyme A 6X 0.01g, *Dulcamara
    2X 0.08g, *Embryo suis 2X 0.001g (Final concentration 7X),
    *Funiculus umbilicalis suis 2X 0.001g (Final concentration 7X)
    Nadidum 6X 0.01g, Natrum oxalaceticum 6X 0.01g, *Placenta
    totalis suis 2X 0.001g (Final concentration 7X), *Rhus toxicodendron
    2X 0.27g (Final concentration 4X), *Sanguinaria canadensis 2X
    0.23g (Final concentration 4X), *Silicea 6X 1g, *Sulphur 6X 0.27g,
    *Symphytum officinale 8X 0.75g. *Natural Ingredient

  • PRINCIPAL DISPLAY PANEL

    Zeel Ointment.jpg

  • INGREDIENTS AND APPEARANCE
    ZEEL 
    alpha lipoic acid, arnica montana whole,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,coriander ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51885-9489
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y) (.ALPHA.-LIPOIC ACID - UNII:73Y7P0K73Y) ALPHA LIPOIC ACID6 [hp_X]  in 1 g
    ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA WHOLE2 [hp_X]  in 1 g
    SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (SUS SCROFA CARTILAGE - UNII:73ECW5WG2F) SUS SCROFA CARTILAGE2 [hp_X]  in 1 g
    COENZYME A (UNII: SAA04E81UX) (COENZYME A - UNII:SAA04E81UX) COENZYME A6 [hp_X]  in 1 g
    SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP2 [hp_X]  in 1 g
    SUS SCROFA EMBRYO (UNII: 9928MC12VO) (SUS SCROFA EMBRYO - UNII:9928MC12VO) SUS SCROFA EMBRYO2 [hp_X]  in 1 g
    SUS SCROFA UMBILICAL CORD (UNII: 118OYG6W3H) (SUS SCROFA UMBILICAL CORD - UNII:118OYG6W3H) SUS SCROFA UMBILICAL CORD2 [hp_X]  in 1 g
    NADIDE (UNII: 0U46U6E8UK) (NADIDE - UNII:0U46U6E8UK) NADIDE6 [hp_X]  in 1 g
    SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (DIETHYL OXALACETATE - UNII:15S56468G7) SODIUM DIETHYL OXALACETATE6 [hp_X]  in 1 g
    SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8) SUS SCROFA PLACENTA2 [hp_X]  in 1 g
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF2 [hp_X]  in 1 g
    SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508) SANGUINARIA CANADENSIS ROOT2 [hp_X]  in 1 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 [hp_X]  in 1 g
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR6 [hp_X]  in 1 g
    CORIANDER (UNII: 1OV56052IK) (CORIANDER - UNII:1OV56052IK) CORIANDER8 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    ALCOHOL (UNII: 3K9958V90M)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51885-9489-81 in 1 CARTON09/22/2021
    1100 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/22/2021
    Labeler - Biologische Heilmittel Heel (315635359)
    Establishment
    NameAddressID/FEIBusiness Operations
    Biologische Heilmittel Heel315635359manufacture(51885-9489)
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