United States · FDA National Drug Code directory
Spleen-Pro T018
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71742-0012_53f1621b-b6d5-4b35-baf3-1657e67cd5c1
- Product NDC
- 71742-0012
- Form
- LIQUID
- Composition / generic term
- Spleen (Suis), Arsenicum Album, Carbo Vegetabilis, Ceanothus Americanus, Chininum Sulphuricum, Ignatia Amara, Iodium, Natrum Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Phosphorus
- Labeler
- Guangzhou Renuma Medical Systems Co., Ltd
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20171026
- Source listing expiry
- 20261231
Source-listed ingredients
- SUS SCROFA SPLEEN — 6 [hp_X]/mL
- ARSENIC TRIOXIDE — 12 [hp_X]/mL
- ACTIVATED CHARCOAL — 12 [hp_X]/mL
- CEANOTHUS AMERICANUS LEAF — 12 [hp_X]/mL
- QUININE SULFATE — 12 [hp_X]/mL
- STRYCHNOS IGNATII SEED — 12 [hp_X]/mL
- IODINE — 12 [hp_X]/mL
- SODIUM CHLORIDE — 12 [hp_X]/mL
- NITRIC ACID — 12 [hp_X]/mL
- PHOSPHORIC ACID — 12 [hp_X]/mL
- PHOSPHORUS — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 59 mL in 1 BOTTLE, DROPPER (71742-0012-1) · 71742-0012-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →