NDC product
Spleen-Pro T018
NDC 71742-0012 · Guangzhou Renuma Medical Systems Co., Ltd
Key facts
| Product NDC | 71742-0012 |
|---|---|
| Proprietary name | Spleen-Pro |
| Nonproprietary name | Spleen (Suis), Arsenicum Album, Carbo Vegetabilis, Ceanothus Americanus, Chininum Sulphuricum, Ignatia Amara, Iodium, Natrum Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Phosphorus |
| Substances | SUS SCROFA SPLEEN, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, CEANOTHUS AMERICANUS LEAF, QUININE SULFATE, STRYCHNOS IGNATII SEED, IODINE, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORIC ACID, PHOSPHORUS |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Guangzhou Renuma Medical Systems Co., Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Antimalarial [EPC] |
| 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: