71742-0011 NDC - KIDNEY-PRO (BERBERIS VULGARIS, PETROSELINUM SATIVUM, SABAL SERRULATA, UVA URSI, CANTHARIS, LITHIUM CARBONICUM, MERCURIUS CORROSIVUS, PAREIRA BRAVA, SARSAPARILLA (SMILAX REGELII), SOLIDAGO VIRGAUREA)

Drug Information

Product NDC: 71742-0011

Proprietary Name: Kidney-Pro

Non Proprietary Name: Berberis Vulgaris, Petroselinum Sativum, Sabal Serrulata, Uva Ursi, Cantharis, Lithium Carbonicum, Mercurius Corrosivus, Pareira Brava, Sarsaparilla (Smilax Regelii), Solidago Virgaurea

Active Ingredient(s):
  • 3 [hp_X]/mL ARCTOSTAPHYLOS UVA-URSI LEAF;
  • 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 12 [hp_X]/mL CHONDRODENDRON TOMENTOSUM ROOT;
  • 12 [hp_X]/mL LITHIUM CARBONATE;
  • 12 [hp_X]/mL LYTTA VESICATORIA;
  • 12 [hp_X]/mL MERCURIC CHLORIDE;
  • 3 [hp_X]/mL PETROSELINUM CRISPUM WHOLE;
  • 3 [hp_X]/mL SAW PALMETTO;
  • 12 [hp_X]/mL SMILAX ORNATA ROOT;
  • 12 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Mood Stabilizer [EPC]

Labeler Information

Labeler Name: Guangzhou Renuma Medical Systems Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/26/2017

Package Information

No. Package Code Package Description Billing Unit
171742-0011-159 mL in 1 BOTTLE, DROPPER (71742-0011-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71742-0011The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEKidney-ProThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXT017A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEBerberis Vulgaris, Petroselinum Sativum, Sabal Serrulata, Uva Ursi, Cantharis, Lithium Carbonicum, Mercurius Corrosivus, Pareira Brava, Sarsaparilla (Smilax Regelii), Solidago VirgaureaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/26/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEGuangzhou Renuma Medical Systems Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARCTOSTAPHYLOS UVA-URSI LEAF; BERBERIS VULGARIS ROOT BARK; CHONDRODENDRON TOMENTOSUM ROOT; LITHIUM CARBONATE; LYTTA VESICATORIA; MERCURIC CHLORIDE; PETROSELINUM CRISPUM WHOLE; SAW PALMETTO; SMILAX ORNATA ROOT; SOLIDAGO VIRGAUREA FLOWERING TOPAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 3; 12; 12; 12; 12; 3; 3; 12; 12 
ACTIVE INGRED UNIT[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 
PHARM CLASSESMood Stabilizer [EPC] 

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This page was last updated on: 2/1/2023