Label: BORAGO LAVENDER CUM CUPRO lotion

  • 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 October 27, 2021

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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: 100gm contains: 20gm Aesculus (Horse chestnut seed) 1X, 20gm Borago (Borage) 1X, 13gm Melilotus (Yellow sweet clover) 1X, 40gm Cuprum sulfuricum (Copper sulfate) 2X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Witch hazel extract, Magnesium aluminum silicate, Lavender oil, Silica gel, Sorbic acid, Tea tree oil, Xanthan gum, Grapefruit seed extract

  • PURPOSE

    Uses: Temporarily relieves symptoms of varicose veins and leg cramps.

  • 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. May leave a therapeutic white residue of silica.

  • QUESTIONS

    Questions? Call 866.642.2858
    Made with care by Uriel, East Troy, WI 53120
    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Borago Lavender cum Cupro Lotion

  • INGREDIENTS AND APPEARANCE
    BORAGO LAVENDER CUM CUPRO 
    borago lavender cum cupro lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2143
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MELILOTUS INDICUS SEED (UNII: F22I9R6Q0X) (MELILOTUS INDICUS SEED - UNII:F22I9R6Q0X) MELILOTUS INDICUS SEED1 [hp_X]  in 1 g
    CUPRIC SULFATE (UNII: LRX7AJ16DT) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION2 [hp_X]  in 1 g
    BORAGE (UNII: PB618V0K2W) (BORAGE - UNII:PB618V0K2W) BORAGE1 [hp_X]  in 1 g
    HORSE CHESTNUT (UNII: 3C18L6RJAZ) (HORSE CHESTNUT - UNII:3C18L6RJAZ) HORSE CHESTNUT1 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    WATER (UNII: 059QF0KO0R)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SORBIC ACID (UNII: X045WJ989B)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-2143-5100 g in 1 BOTTLE, GLASS; 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(48951-2143)
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