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
Venapro
FDA Label NDC 43695-0003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pacific Naturals for the product Venapro (NDC 43695-0003). 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 active ingredients:, indications:, warnings:, keep out of reach of children:, directions:, inactive ingredients:, questions:, package label display:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications:
Treats symptoms associated with hemorrhoids.
Treats symptoms associated with hemorrhoids.
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.
Keep Out Of Reach Of Children:
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions:
Adults and Children over 12: Spray twice under the tongue 3 times per day.
Children under 12: Consult a doctor prior to use.
Inactive Ingredients:
Alcohol 26% v/v, Purified water.
Questions:
Distributed By: Pacific Naturals
Unit 40 Tanners Drive, Blakelands
Milton Keynes, UK MK14 5BW, United Kingdom
Phone: 1-877-320-0266
Package Label Display:
Venapro
Hemorrhoid Relief
HOMEOPATHIC
1.0 FL OZ. (30 ml)
* Please review the disclaimer below.
