Label: ANGELICA COMP. 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 April 10, 2018

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: Angelica 1X, Echinacea (Purple coneflower) 1X, Levisticum (Lovage) 2X, Spilanthes (Toothache plant) 2X, Calendula 3X, Cuprum aceticum (Copper acetate) 3X, Inula helen. (Elecampane) 6X, Plantago (Ribwort plantain) 6X, Verbascum (Great mullein) 6X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, 20% 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 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 www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    AngelicaComp.Liquid

  • INGREDIENTS AND APPEARANCE
    ANGELICA COMP. 
    angelica comp. liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1035
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (ANGELICA ARCHANGELICA ROOT - UNII:DTN01M69SN) ANGELICA ARCHANGELICA ROOT1 [hp_X]  in 1 mL
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA1 [hp_X]  in 1 mL
    LEVISTICUM OFFICINALE ROOT (UNII: 46QZ19OEX8) (LEVISTICUM OFFICINALE ROOT - UNII:46QZ19OEX8) LEVISTICUM OFFICINALE ROOT2 [hp_X]  in 1 mL
    ACMELLA OLERACEA WHOLE (UNII: G5914Q15B6) (ACMELLA OLERACEA WHOLE - UNII:G5914Q15B6) ACMELLA OLERACEA WHOLE2 [hp_X]  in 1 mL
    CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP3 [hp_X]  in 1 mL
    CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC ACETATE3 [hp_X]  in 1 mL
    INULA HELENIUM ROOT (UNII: E55SMD6DA8) (INULA HELENIUM ROOT - UNII:E55SMD6DA8) INULA HELENIUM ROOT6 [hp_X]  in 1 mL
    PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X) PLANTAGO MAJOR LEAF6 [hp_X]  in 1 mL
    VERBASCUM DENSIFLORUM LEAF (UNII: 9936O846LI) (VERBASCUM DENSIFLORUM LEAF - UNII:9936O846LI) VERBASCUM DENSIFLORUM LEAF6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1035-360 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(48951-1035)