Venapro by Liddell Laboratories, Inc. VENAPRO spray

Venapro by

Drug Labeling and Warnings

Venapro by is a Homeopathic medication manufactured, distributed, or labeled by Liddell Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

INDICATIONS:  Treats symptoms associated with hemorrhoids.

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.

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.

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.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:   Alcohol 26%, Purified water

PRINCIPAL DISPLAY PANEL

VENAPRO

Hemorrhoid Relief

HOMEOPATHIC

1.0 FL OZ. (30 ML)

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