DROSERA COMP. LIQUID [URIEL PHARMACY INC.]

DROSERA COMP. LIQUID [URIEL PHARMACY INC.]
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NDC 48951-4009-3
Set ID cfb0332c-1a02-4f0a-9f5d-0bbae4fa3af2
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Drosera (Sundew) 3X, Atropa belladonna (Nightshade) 4X, China (Peruvian bark) 4X, Coccus cacti (Cochineal bug, female) 4X, Helleborus (Christmas rose) 4X, Ipecacuanha (Ipecac) 4X, Mephitis (Secretion from the rectal gland of skunk) 4X, Veratrum (White hellebore) 4X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Organic cane alcohol

  • PURPOSE

    Use: Temporary relief of cough.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: 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 conditons or if conditons worsen or persist. If pregnant or nursing, consult a doctor before use. 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

    DroseraCompLiquid

  • INGREDIENTS AND APPEARANCE
    DROSERA COMP. 
    drosera comp. liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-4009
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA3 [hp_X]  in 1 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA4 [hp_X]  in 1 mL
    QUILLAJA SAPONARIA BARK (UNII: 8N0K3807ZW) (QUILLAJA SAPONARIA BARK - UNII:8N0K3807ZW) QUILLAJA SAPONARIA BARK4 [hp_X]  in 1 mL
    PROTORTONIA CACTI (UNII: LZB7TFX1LT) (PROTORTONIA CACTI - UNII:LZB7TFX1LT) PROTORTONIA CACTI4 [hp_X]  in 1 mL
    HELLEBORUS FOETIDUS ROOT (UNII: 332Y7EES96) (HELLEBORUS FOETIDUS ROOT - UNII:332Y7EES96) HELLEBORUS FOETIDUS ROOT4 [hp_X]  in 1 mL
    IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC4 [hp_X]  in 1 mL
    MEPHITIS MEPHITIS ANAL GLAND FLUID (UNII: 3BN57UN4US) (MEPHITIS MEPHITIS ANAL GLAND FLUID - UNII:3BN57UN4US) MEPHITIS MEPHITIS ANAL GLAND FLUID4 [hp_X]  in 1 mL
    VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z) VERATRUM ALBUM ROOT4 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-4009-360 mL in 1 BOTTLE, DROPPER; 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(48951-4009)

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