Otc - Purpose
INDICATIONS: Treats symptoms associated with hemorrhoids.
Venapro
FDA Label NDC 50845-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Liddell Laboratories, Inc. for the product Venapro (NDC 50845-0002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - purpose, dosage & administration, warnings, otc - active ingredient, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Otc - 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
Package Label.Principal Display Panel
VENAPRO
Hemorrhoid Relief
HOMEOPATHIC
1.0 FL OZ. (30 ML)
Venapro (Mm1)
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