Label: VENAPRO - venapro spray

  • NDC Code(s): 50845-0002-1
  • Packager: Liddell Laboratories, Inc.
  • 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 June 16, 2010

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

  • PURPOSE

    INDICATIONS:  Treats symptoms associated with hemorrhoids.


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  • DOSAGE & ADMINISTRATION

    DIRECTIONS:  Adults and children over 12:  Spray twice under the tongue 3 times per day.  Children under 12:  Consult a doctor prior to use.


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  • WARNINGS

    WARNINGS:  If symptoms persist, consult a doctor.  In case of overdose, get medical help or contact a Poison Control Center right away.  If pregnant or breast-feeding, ask a doctor before use.

    DO NOT use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

    Keep out of reach of children.





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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Aesculus hippocastanum 1X, Arnica montana 3X, Calcarea fluorica 10X, Carduus marianus 1X, Collinsonia canadensis 3X, Hamamelis virginiana 1X, Muriaticum acidum 6X, Ratanhia 3X.


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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:   Alcohol 26%, Purified water

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  • PRINCIPAL DISPLAY PANEL

    VENAPRO

    Hemorrhoid Relief

    HOMEOPATHIC

    1.0 FL OZ. (30 ML)

    Venapro

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  • INGREDIENTS AND APPEARANCE
    VENAPRO 
    venapro spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50845-0002
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HORSE CHESTNUT (UNII: 3C18L6RJAZ) (HORSE CHESTNUT - UNII:3C18L6RJAZ) HORSE CHESTNUT 1 [hp_X]  in 1 mL
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 3 [hp_X]  in 1 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM FLUORIDE 10 [hp_X]  in 1 mL
    SILYBUM MARIANUM SEED (UNII: U946SH95EE) (SILYBUM MARIANUM SEED - UNII:U946SH95EE) SILYBUM MARIANUM SEED 1 [hp_X]  in 1 mL
    COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (COLLINSONIA CANADENSIS ROOT - UNII:O2630F3XDR) COLLINSONIA CANADENSIS ROOT 3 [hp_X]  in 1 mL
    HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 1 [hp_X]  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB) (HYDROCHLORIC ACID - UNII:QTT17582CB) HYDROCHLORIC ACID 6 [hp_X]  in 1 mL
    KRAMERIA LAPPACEA ROOT (UNII: P29ZH1A35Z) (KRAMERIA LAPPACEA ROOT - UNII:P29ZH1A35Z) KRAMERIA LAPPACEA ROOT 3 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50845-0002-1 30 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 05/12/2010
    Labeler - Liddell Laboratories, Inc. (832264241)
    Establishment
    Name Address ID/FEI Business Operations
    Liddell Laboratories, Inc. 832264241 manufacture
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