NDC product
Glucose Control T015
NDC 71742-0009 · Guangzhou Renuma Medical Systems Co., Ltd
Key facts
| Product NDC | 71742-0009 |
|---|---|
| Proprietary name | Glucose Control |
| Nonproprietary name | Syzygium Jambolanum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Hypophysis Suis, Pancreas Suis, Phaseolus, Aceticum Acidum, Lacticum Acidum, Phosphoricum Acidum, Phosphorus, Uranium Nitricum |
| Substances | SYZYGIUM CUMINI SEED, SUS SCROFA ADRENAL GLAND, GOLDENSEAL, SUS SCROFA PITUITARY GLAND, SUS SCROFA PANCREAS, KIDNEY BEAN, ACETIC ACID, LACTIC ACID, PHOSPHORIC ACID, PHOSPHORUS, URANYL NITRATE HEXAHYDRATE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Guangzhou Renuma Medical Systems Co., Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| 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] and 2 more |
| Marketing start | Oct 26, 2017 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: