Label: BAMBUSA AESCULUS- bambusa vulgaris whole, stachys officinalis, rosmarinus officinalis flowering top, formica rufa, bos taurus intervertebral disc, silicon dioxide, arnica montana and horse chestnut gel 

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  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 11/13

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    Directions:  Under age 2: Consult a doctor.

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  • DOSAGE & ADMINISTRATION

    Apply gel to skin as needed.

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  • ACTIVE INGREDIENT

    Active Ingredients: Bambusa e nodo 6X, Betonica
    ex herba 6X, Rosmarinus ex herba 6X, Formica ex animale 7X, Disci intervertebrales 8X, Jasper 12X, Arnica e pl. tota 20X, Aesculus e sem. 50X

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  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Glycerin, Sodium alginate, Lavender oil, Rosemary oil, Potassium sorbate, Grapefruit seed extract

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  • PURPOSE

    Use: Temporary relief of headache.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

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  • WARNINGS

    Warnings: FOR EXTERNAL USE ONLY.
    Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing. Avoid contact with eyes. Natural ingredients may cause color and/or scent variation.

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  • QUESTIONS

    Questions? Call 866.642.2858
    Made with care by Uriel, East Troy, WI 53120
    www.urielpharmacy.com

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  • INGREDIENTS AND APPEARANCE
    BAMBUSA AESCULUS 
    bambusa aesculus gel
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:48951-2003
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BAMBUSA VULGARIS WHOLE (BAMBUSA VULGARIS WHOLE) BAMBUSA VULGARIS WHOLE 6 [hp_X]  in 1 g
    STACHYS OFFICINALIS (STACHYS OFFICINALIS) STACHYS OFFICINALIS 6 [hp_X]  in 1 g
    ROSMARINUS OFFICINALIS FLOWERING TOP (ROSMARINUS OFFICINALIS FLOWERING TOP) ROSMARINUS OFFICINALIS FLOWERING TOP 6 [hp_X]  in 1 g
    FORMICA RUFA (FORMICA RUFA) FORMICA RUFA 7 [hp_X]  in 1 g
    BOS TAURUS INTERVERTEBRAL DISC (BOS TAURUS INTERVERTEBRAL DISC) BOS TAURUS INTERVERTEBRAL DISC 8 [hp_X]  in 1 g
    SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE 12 [hp_X]  in 1 g
    ARNICA MONTANA (ARNICA MONTANA) ARNICA MONTANA 20 [hp_X]  in 1 g
    HORSE CHESTNUT (HORSE CHESTNUT) HORSE CHESTNUT 50 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    GLYCERIN  
    SODIUM ALGINATE  
    LAVENDER OIL  
    ROSEMARY OIL  
    POTASSIUM SORBATE  
    CITRUS PARADISI SEED  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-2003-5 60 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - URIEL PHARMACY INC. (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    URIEL PHARMACY INC. 043471163 manufacture(48951-2003)
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