BAMBUSA ARGENTUM GEL [URIEL PHARMACY INC.]

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BAMBUSA ARGENTUM GEL [URIEL PHARMACY INC.]
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NDC 48951-2006-5
Set ID 2e11a55c-20b4-466d-a313-2f008f53b5c2
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
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  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Apply to skin as needed. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Bambusa (Bamboo) 8X, Betonica (Wood betony) 8X, Rosmarinus (Rosemary) 8X, Aurum met. (Metallic gold) 9X, Disci intervert. (Bovine intervertebral discs of the cervical, thoracic and lumbar spine) 10X, Cuprum met. (Copper) 11X, Jasper (Semiprecious stone) 19X, Argentum met. (Silver) 22X, Arnica 22X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Glycerin, Boric acid, Sodium alginate, Lavender oil, Sodium hydroxide,
    Sorbic acid, Tea tree oil, Grapefruit seed extract

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: FOR EXTERNAL USE ONLY.
    Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.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. Avoid contact with eyes. Do not use if safety seal is broken or missing.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Bambusa Argentum gel

  • INGREDIENTS AND APPEARANCE
    BAMBUSA ARGENTUM 
    bambusa argentum gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2138
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK) (BAMBUSA VULGARIS WHOLE - UNII:WCD45M1BSK) BAMBUSA VULGARIS WHOLE8 [hp_X]  in 1 g
    STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N) STACHYS OFFICINALIS8 [hp_X]  in 1 g
    ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79) ROSMARINUS OFFICINALIS FLOWERING TOP8 [hp_X]  in 1 g
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD9 [hp_X]  in 1 g
    BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (BOS TAURUS INTERVERTEBRAL DISC - UNII:0A04Z76C13) BOS TAURUS INTERVERTEBRAL DISC10 [hp_X]  in 1 g
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER11 [hp_X]  in 1 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE19 [hp_X]  in 1 g
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER22 [hp_X]  in 1 g
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA22 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBIC ACID (UNII: X045WJ989B)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-2138-560 g in 1 TUBE; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-2138)
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