Kidney-Pro

Product NDC
71742-0011
11-digit product format
717420011
Labeler code
71742
Product ID
71742-0011_dcc3be8f-d360-4cc6-903a-d8a80eaa2f03
Type
HUMAN OTC DRUG
Nonproprietary name
Berberis Vulgaris, Petroselinum Sativum, Sabal Serrulata, Uva Ursi, Cantharis, Lithium Carbonicum, Mercurius Corrosivus, Pareira Brava, Sarsaparilla (Smilax Regelii), Solidago Virgaurea
Dosage form
LIQUID
Route
ORAL
Labeler
Guangzhou Renuma Medical Systems Co., Ltd
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-10-26
Marketing end
0000-00-00
Substance
BERBERIS VULGARIS ROOT BARK; PETROSELINUM CRISPUM WHOLE; SAW PALMETTO; ARCTOSTAPHYLOS UVA-URSI LEAF; LYTTA VESICATORIA; LITHIUM CARBONATE; MERCURIC CHLORIDE; CHONDRODENDRON TOMENTOSUM ROOT; SMILAX ORNATA ROOT; SOLIDAGO VIRGAUREA FLOWERING TOP
Active strength
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
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71742-0011DDiscontinued by firm2026-07-31
excluded packagepackage71742-001171742-0011-1DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71742-0011-17174200110159 mL in 1 BOTTLE, DROPPER (71742-0011-1) 59 ml2017-10-260000-00-00NoNoCurrent