Label: ROBINIA NICOTIANA liquid

  • 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 November 3, 2023

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

  • 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: Robinia 4X, Argentum nitricum (Silver nitrate) 6X, Nicotiana (Tobacco) 6X, Nux vomica (Poison nut) 6X, Gl. suprarenales (Bovine adrenal gland)8X, Cuprum met. (Copper) 8X,Natrium phos.(Sodium monohydrogenphosphate) 10X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose

  • PURPOSE

    Use: Temporary relief of upset stomach.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Contains traces of lactose. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions 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
    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Robinia Nicotiana Liquid

  • INGREDIENTS AND APPEARANCE
    ROBINIA NICOTIANA 
    robinia nicotiana liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8397
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF6 [hp_X]  in 1 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED6 [hp_X]  in 1 mL
    BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (BOS TAURUS ADRENAL GLAND - UNII:M2776SWB29) BOS TAURUS ADRENAL GLAND8 [hp_X]  in 1 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER8 [hp_X]  in 1 mL
    SODIUM PHOSPHATE (UNII: SE337SVY37) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE10 [hp_X]  in 1 mL
    ROBINIA PSEUDOACACIA BARK (UNII: 7TPC058OWY) (ROBINIA PSEUDOACACIA BARK - UNII:7TPC058OWY) ROBINIA PSEUDOACACIA BARK4 [hp_X]  in 1 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8397-360 mL 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(48951-8397)