Lymphdrainex
- Product NDC
- 44911-0533
- Requested package NDC
- 44911-0533-1
- 11-digit product format
- 449110533
- Labeler code
- 44911
- Product ID
- 44911-0533_fed4ad0c-e899-4113-ab93-44c97e5f5239
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Geranium Robertianum, Nasturtium Aquaticum, Scrophularia Nodosa, Teucrium Scorodonia, Apis Mellifica, Equisetum Hyemale, Fumaria Officinalis, Natrum Sulphuricum, Phytolacca Decandra, Pinus Sylvestris, Veronica Officinalis, Aloe, Gentiana Lutea, Sarsaparilla (Smilax Regelii), Baryta Carbonica, Hepar Sulphuris Calcareum, Mercurius Cyanatus, Ferrum Iodatum, Myosotis Arvensis, Aranea Diadema, Calcarea Phosphorica, Juglans Regia, Parathyroid Gland (Bovine), Thymus (Suis), Thyroidinum (Suis)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-02-26
- Marketing end
- 2025-02-24
- Substance
- GERANIUM ROBERTIANUM; NASTURTIUM OFFICINALE; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; APIS MELLIFERA; EQUISETUM HYEMALE; FUMARIA OFFICINALIS FLOWERING TOP; SODIUM SULFATE; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS LEAFY TWIG; VERONICA OFFICINALIS FLOWERING TOP; ALOE; GENTIANA LUTEA ROOT; SMILAX ORNATA WHOLE; BARIUM CARBONATE; CALCIUM SULFIDE; MERCURIC CYANIDE; FERROUS IODIDE; MYOSOTIS ARVENSIS; ARANEUS DIADEMATUS; TRIBASIC CALCIUM PHOSPHATE; JUGLANS REGIA LEAF; BOS TAURUS PARATHYROID GLAND; SUS SCROFA THYMUS; SUS SCROFA THYROID
- Active strength
- 3 [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; [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 | 44911-0533 | 44911-0533-1 | 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… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 44911-0533-1 | 44911053301 | 60 mL in 1 BOTTLE, DROPPER (44911-0533-1) | 60 ml | 2020-02-26 | 2025-02-24 | No | No | Current |