Home NDC 44911-0460-1 Lymphdrainex
Product NDC 44911-0460
Requested package NDC 44911-0460-1
11-digit product format 449110460
Labeler code 44911
Product ID 44911-0460_b348841f-283b-4fd7-bac2-eed23e2887d6
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, Juglans Regia, Myosotis Arvensis, Sarsaparilla (Smilax Regelii), Baryta Carbonica, Hepar Sulphuris Calcareum, Mercurius Cyanatus, Ferrum Iodatum, Aranea Diadema, Calcarea Phosphorica, Parathyroid Gland (Bovine), Thymus (Suis), Thyroidinum (Suis)
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-07-17
Marketing end 2023-08-27
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; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; MYOSOTIS ARVENSIS; SMILAX ORNATA ROOT; BARIUM CARBONATE; CALCIUM SULFIDE; MERCURIC CYANIDE; FERROUS IODIDE; ARANEUS DIADEMATUS; TRIBASIC CALCIUM PHOSPHATE; 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; [hp_X]/mL
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table 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.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0460-1 44911046001 60 mL in 1 BOTTLE, DROPPER (44911-0460-1) 60 ml 2018-07-17 2023-08-27 No No Current