RUMEX OBTUSIFOLIUS (RUMEX OBTUSIFOLIUS ROOT) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]

  • Home
  • RUMEX OBTUSIFOLIUS (RUMEX OBTUSIFOLIUS ROOT) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]

RUMEX OBTUSIFOLIUS (RUMEX OBTUSIFOLIUS ROOT) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS]
PDF | XML
NDC 71919-594-07, 71919-594-08, 71919-594-09, 71919-594-10
Set ID 3729a490-a42f-4d6b-a72c-58b4f12cb0ce
Category HUMAN OTC DRUG LABEL
Packager Washington Homeopathic Products
Generic Name
Product Class
Product Number
Application Number
View All Sections
  • ACTIVE INGREDIENTS

    RUMEX OBTUS

  • USES

    To relieve the symptoms of nosebleeds.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of reach of children.

  • INDICATIONS

    Indications: 

    RUMEX OBTUS   Nosebleeds

  • STOP USE AND ASK DOCTOR

    If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

  • DIRECTIONS

    Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

  • INACTIVE INGREDIENTS

    Sucrose/Lactose

  • PRINCIPAL DISPLAY PANEL

    The OTC potency range of RUMEX OBTUS is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

    Availability is subject to change.

    LABEL

    All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

    ‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

    Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

  • INGREDIENTS AND APPEARANCE
    RUMEX OBTUSIFOLIUS 
    rumex obtusifolius root liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71919-594
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RUMEX OBTUSIFOLIUS ROOT (UNII: 49312EBI2S) (RUMEX OBTUSIFOLIUS ROOT - UNII:49312EBI2S) RUMEX OBTUSIFOLIUS ROOT30 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (white) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71919-594-0715 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product10/06/2011
    2NDC:71919-594-0830 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product10/06/2011
    3NDC:71919-594-0950 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product10/06/2011
    4NDC:71919-594-10100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product10/06/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/06/2011
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    NameAddressID/FEIBusiness Operations
    Washington Homeopathic Products084929389manufacture(71919-594)
View All Sections

Related Drugs

Search DailyMed Drugs