NDC 71742-0003 Vascu-pro T009

Cactus Grandiflorus, Hamamelis Virginiana, Valeriana Officinalis, Arteria Suis, Heart (suis), Arnica Montana, Aurum Metallicum, Baryta Muriatica, Cholesterinum, Lecithin, Magnesia Muriatica, Oxalicum Acidum, Phosphorus

NDC Product Code 71742-0003

NDC Product Information

Vascu-pro T009 with NDC 71742-0003 is a a human over the counter drug product labeled by Guangzhou Renuma Medical Systems Co., Ltd. The generic name of Vascu-pro T009 is cactus grandiflorus, hamamelis virginiana, valeriana officinalis, arteria suis, heart (suis), arnica montana, aurum metallicum, baryta muriatica, cholesterinum, lecithin, magnesia muriatica, oxalicum acidum, phosphorus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Guangzhou Renuma Medical Systems Co., Ltd

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Vascu-pro T009 Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • VALERIAN 3 [hp_X]/mL
  • PORK HEART 6 [hp_X]/mL
  • ARNICA MONTANA 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • CHOLESTEROL 12 [hp_X]/mL
  • LECITHIN, SOYBEAN 12 [hp_X]/mL
  • OXALIC ACID 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Guangzhou Renuma Medical Systems Co., Ltd
Labeler Code: 71742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-19-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Vascu-pro T009 Product Label Images

Vascu-pro T009 Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Cactus Grandiflorus 3X, Hamamelis Virginiana 3X, Valeriana Officinalis 3X, Arteria Suis 6X, Heart (Suis) 6X, Arnica Montana 12X, Aurum Metallicum 12X, Baryta Muriatica 12X, Cholesterinum 12X, Lecithin 12X, Magnesia Muriatica 12X, Oxalicum Acidum 12X, Phosphorus 12X.


May temporarily relieve cold clammy feet, numbness of limbs, painful calves upon walking, muscular weakness of the lower extremities.

May temporarily relieve cold clammy feet, numbness of limbs, painful calves upon walking, muscular weakness of the lower extremities.


If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in cool, dry place.

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.


Adults and children 5 to 10 drops orally, 1 to 2 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, Glycerin


Distributed by:Guangzhou Renuma MedicalSystems Co., Ltd.No. 5, 2nd Floor, Ascendas 2nd StreetSino-Singapore Guangzhou Knowledge CityGuangzhou 510555, China

Package Label Display:

VASCU-PROT009HOMEOPATHIC2 fl. oz. (59 ml)

* Please review the disclaimer below.