Search by Drug Name or NDC

NDC 71742-0003-01 Vascu-Pro 12; 12; 12; 12; 3; 12; 12; 12; 12; 6; 3; 6; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

Vascu-Pro 12; 12; 12; 12; 3; 12; 12; 12; 12; 6; 3; 6; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Vascu-Pro is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Guangzhou Renuma Medical Systems Co., Ltd. The primary component is ARNICA MONTANA; BARIUM CHLORIDE DIHYDRATE; CHOLESTEROL; GOLD; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; LECITHIN, SOYBEAN; MAGNESIUM CHLORIDE; OXALIC ACID; PHOSPHORUS; PORK HEART; SELENICEREUS GRANDIFLORUS STEM; SUS SCROFA ARTERY; VALERIAN.

Product Information

NDC	71742-0003
Product ID	71742-0003_07ceb79a-af82-4cc1-89cf-8263c9dea39d
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Vascu-Pro
Proprietary Name Suffix	T009
Non-Proprietary Name	Cactus Grandiflorus, Hamamelis Virginiana, Valeriana Officinalis, Arteria Suis, Heart (Suis), Arnica Montana, Aurum Metallicum, Baryta Muriatica, Cholesterinum, Lecithin, Magnesia Muriatica, Oxalicum Acidum, Phosphorus
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	12; 12; 12; 12; 3; 12; 12; 12; 12; 6; 3; 6; 3
Active Ingredient Units	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Substance Name	ARNICA MONTANA; BARIUM CHLORIDE DIHYDRATE; CHOLESTEROL; GOLD; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; LECITHIN, SOYBEAN; MAGNESIUM CHLORIDE; OXALIC ACID; PHOSPHORUS; PORK HEART; SELENICEREUS GRANDIFLORUS STEM; SUS SCROFA ARTERY; VALERIAN
Labeler Name	Guangzhou Renuma Medical Systems Co., Ltd
Pharmaceutical Class	Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electr
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 71742-0003-01 (71742000301)

Pricing Information	N/A
NDC Package Code	71742-0003-1
Billing NDC	71742000301
Package	59 mL in 1 BOTTLE, DROPPER (71742-0003-1)
Marketing Start Date	2017-10-19
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 01d22fd6-7d2f-4448-81ff-c88baafc0af7 Details

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.

INDICATIONS:

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

WARNINGS:

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.

DIRECTIONS:

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.

INDICATIONS:

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

INACTIVE INGREDIENTS:

Demineralized water, Glycerin

QUESTIONS:

Distributed by:

Guangzhou Renuma Medical

Systems Co., Ltd.

No. 5, 2nd Floor, Ascendas 2nd Street

Sino-Singapore Guangzhou Knowledge City

Guangzhou 510555, China

PACKAGE LABEL DISPLAY:

VASCU-PRO

T009

HOMEOPATHIC

2 fl. oz. (59 ml)

INGREDIENTS AND APPEARANCE

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 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71742-0003
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK)	SELENICEREUS GRANDIFLORUS STEM	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	3 [hp_X] in 1 mL
VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW)	VALERIAN	3 [hp_X] in 1 mL
SUS SCROFA ARTERY (UNII: 63O327782Q) (SUS SCROFA ARTERY - UNII:63O327782Q)	SUS SCROFA ARTERY	6 [hp_X] in 1 mL
PORK HEART (UNII: X876KJM95L) (PORK HEART - UNII:X876KJM95L)	PORK HEART	6 [hp_X] in 1 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	12 [hp_X] in 1 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	12 [hp_X] in 1 mL
BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E) (BARIUM CATION - UNII:V645272HLN)	BARIUM CHLORIDE DIHYDRATE	12 [hp_X] in 1 mL
CHOLESTEROL (UNII: 97C5T2UQ7J) (CHOLESTEROL - UNII:97C5T2UQ7J)	CHOLESTEROL	12 [hp_X] in 1 mL
LECITHIN, SOYBEAN (UNII: 1DI56QDM62) (LECITHIN, SOYBEAN - UNII:1DI56QDM62)	LECITHIN, SOYBEAN	12 [hp_X] in 1 mL
MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM CATION	12 [hp_X] in 1 mL
OXALIC ACID (UNII: 9E7R5L6H31) (OXALIC ACID - UNII:9E7R5L6H31)	OXALIC ACID	12 [hp_X] in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	12 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71742-0003-1	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/19/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		10/19/2017

Labeler - Guangzhou Renuma Medical Systems Co., Ltd (544538706)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(71742-0003) , api manufacture(71742-0003) , label(71742-0003) , pack(71742-0003)

Revised: 10/2017

Document Id: 07ceb79a-af82-4cc1-89cf-8263c9dea39d

Set id: 01d22fd6-7d2f-4448-81ff-c88baafc0af7

Version: 1

Effective Time: 20171019

Search by Drug Name or NDC

NDC 71742-0003-01 Vascu-Pro 12; 12; 12; 12; 3; 12; 12; 12; 12; 6; 3; 6; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

Vascu-Pro 12; 12; 12; 12; 3; 12; 12; 12; 12; 6; 3; 6; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Product Information

Package

Package Images

NDC 71742-0003-01 (71742000301)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 01d22fd6-7d2f-4448-81ff-c88baafc0af7 Details

ACTIVE INGREDIENTS:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

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