Home NDC 71742-0009 Glucose Control
Product NDC 71742-0009
11-digit product format 717420009
Labeler code 71742
Product ID 71742-0009_5e65d625-8b6c-48af-84c6-f91fdf8cf01d
Type HUMAN OTC DRUG
Nonproprietary name Syzygium Jambolanum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Hypophysis Suis, Pancreas Suis, Phaseolus, Aceticum Acidum, Lacticum Acidum, Phosphoricum Acidum, Phosphorus, Uranium Nitricum
Dosage form LIQUID
Route ORAL
Labeler Guangzhou Renuma Medical Systems Co., Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-10-26
Substance ACETIC ACID; GOLDENSEAL; KIDNEY BEAN; LACTIC ACID; PHOSPHORIC ACID; PHOSPHORUS; SUS SCROFA ADRENAL GLAND; SUS SCROFA PANCREAS; SUS SCROFA PITUITARY GLAND; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE
Active strength 12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 12 [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
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Glucose Control
Brand name suffix T015
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SYZYGIUM CUMINI SEED 12 [hp_X]/mL SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL GOLDENSEAL 9 [hp_X]/mL SUS SCROFA PITUITARY GLAND 12 [hp_X]/mL SUS SCROFA PANCREAS 12 [hp_X]/mL KIDNEY BEAN 12 [hp_X]/mL ACETIC ACID 6 [hp_X]/mL LACTIC ACID 6 [hp_X]/mL PHOSPHORIC ACID 6 [hp_X]/mL PHOSPHORUS 3 [hp_X]/mL URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71742-0009-1 Glucose ControlT015 59 mL in 1 BOTTLE, DROPPER LIQUID 59 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71742-0009 GLUCOSE CONTROL T015 (SYZYGIUM JAMBOLANUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, HYPOPHYSIS SUIS, PANCREAS SUIS, PHASEOLUS, ACETICUM ACIDUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, URANIUM NITRICUM) LIQUID [GUANGZHOU RENUMA MEDICAL SYSTEMS CO., LTD] 1 Current NDC, Legacy NDC, 1 package rows 20171027_3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Glucose Control T015 SYZYGIUM JAMBOLANUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, HYPOPHYSIS SUIS, PANCREAS SUIS, PHASEOLUS, ACETICUM ACIDUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, URANIUM NITRICUM Guangzhou Renuma Medical Systems Co., Ltd 3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b 2017-10-26 Warnings Exact identifier ndc (product): 71742-0009
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71742-0009-1 71742000901 59 mL in 1 BOTTLE, DROPPER (71742-0009-1) 59 ml 2017-10-26 0000-00-00 No No Current