Liver Drainage
- Product NDC
- 43742-0490
- Requested package NDC
- 43742-0490-1
- 11-digit product format
- 437420490
- Labeler code
- 43742
- Product ID
- 43742-0490_d8930949-819a-438c-9c13-5d19235a47cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chelidonium Majus, Carduus Marianus, Schisandra Chinensis, Taraxacum Officinale, Berberis Vulgaris, Neopicrorhiza Scrophulariiflora, Raphanus Sativus, Viscum Album, Chromium Gluconate, Cobalt Gluconate, Copper Gluconate, Magnesium Gluconate, Natrum Sulphuricum, Ptelea Trifoliate, Sarcolacticum Acidum, Sulphur Iodatum, Carbolicum Acidum, Cichorium Intybus, Flos, Gallbladder (Suis), Hepar Suis, Nux Vomica, Pancreas Suis, Vanadium Metallicum, Verbena Officinalis, Flos
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-06-21
- Marketing end
- 2024-05-31
- Substance
- CHELIDONIUM MAJUS; MILK THISTLE; SCHISANDRA CHINENSIS FRUIT; TARAXACUM OFFICINALE; BERBERIS VULGARIS ROOT BARK; NEOPICRORHIZA SCROPHULARIIFLORA ROOT; RADISH; VISCUM ALBUM FRUITING TOP; CHROMIUM GLUCONATE; COBALTOUS GLUCONATE; COPPER GLUCONATE; MAGNESIUM GLUCONATE; SODIUM SULFATE; PTELEA TRIFOLIATA BARK; LACTIC ACID, L-; SULFUR IODIDE; PHENOL; CICHORIUM INTYBUS FLOWER; SUS SCROFA GALLBLADDER; PORK LIVER; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA PANCREAS; VANADIUM; VERBENA OFFICINALIS FLOWERING TOP
- Active strength
- 1 [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; [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; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 43742-0490 | 43742-0490-1 | D | Discontinued by firm | 2026-10-05 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43742-0490-1 | 43742049001 | 60 mL in 1 BOTTLE, DROPPER (43742-0490-1) | 60 ml | 2014-06-21 | 2024-05-31 | No | No | Current |