Label: URICUM ACIDUM- uric acid liquid

  • NDC Code(s): 71919-695-07, 71919-695-08, 71919-695-09, 71919-695-10
  • Packager: Washington Homeopathic Products
  • 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 July 15, 2019

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

  • ACTIVE INGREDIENTS

    URICUM ACIDUM

  • USES

    To relieve the symptoms of minor joint pain.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medicines out of reach of children.

  • INDICATIONS

    Indications:

    URICUM ACIDUM Minor joint pain

  • 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 ALFALFA 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
    URICUM ACIDUM 
    uric acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71919-695
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    URIC ACID (UNII: 268B43MJ25) (URIC ACID - UNII:268B43MJ25) URIC ACID30 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71919-695-0715 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product05/17/2011
    2NDC:71919-695-0830 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product05/17/2011
    3NDC:71919-695-0950 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/17/2011
    4NDC:71919-695-10100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/17/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/17/2011
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    NameAddressID/FEIBusiness Operations
    Washington Homeopathic Products084929389manufacture(71919-695)