Lymphdrainex NDC 44911-0689

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0689Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0689Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0689-1	44911068901	60 mL in 1 BOTTLE, DROPPER (44911-0689-1)Marketed from Dec 28, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Lymphdrainex
Generic name (nonproprietary): geranium robertianum, nasturtium aquaticum, teucrium scorodonia, equisetum hyemale, fumaria officinalis, natrum sulphuricum, phytolacca decandra, pinus sylvestris, veronica officinalis, baptisia tinctoria, galium aparine, gentiana lutea, apis mellifica, sarsaparilla (smilax regelii), baryta carbonica, hepar sulphuris calcareum, mercurius cyanatus, scrophularia nodosa, aloe, ferrum iodatum, myosotis arvensis, aranea diadema, calcarea phosphorica, juglans regia, parathyroid gland (bovine), silicea,
Active ingredients: Geranium robertianum whole — 3 [hp_X]/mLNasturtium officinale — 3 [hp_X]/mLTeucrium scorodonia flowering top — 3 [hp_X]/mLEquisetum hyemale whole — 4 [hp_X]/mLFumaria officinalis flowering top — 4 [hp_X]/mLSodium sulfate — 4 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLPinus sylvestris leafy twig — 4 [hp_X]/mLVeronica officinalis flowering top — 4 [hp_X]/mLBaptisia tinctoria root — 5 [hp_X]/mLGalium aparine whole — 5 [hp_X]/mLGentiana lutea root — 5 [hp_X]/mLApis mellifera — 6 [hp_X]/mLSmilax ornata root — 6 [hp_X]/mLBarium carbonate — 8 [hp_X]/mLCalcium sulfide — 8 [hp_X]/mLMercuric cyanide — 8 [hp_X]/mLScrophularia nodosa whole — 8 [hp_X]/mLAloe — 8 [hp_X]/mLFerrous iodide — 8 [hp_X]/mLMyosotis arvensis whole — 10 [hp_X]/mLAraneus diadematus — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLJuglans regia fruit rind, Immature — 12 [hp_X]/mLJuglans regia leaf — 12 [hp_X]/mLBos taurus parathyroid gland — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSus scrofa thymus — 12 [hp_X]/mLThyroid — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 28, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 44911-0689_1946434d-d66f-4a82-a357-6614aaaf332eSPL ID 1946434d-d66f-4a82-a357-6614aaaf332eSPL set ID c512f211-f4f8-46f6-87ed-dd50287359dfUNII R5I1HK0UBL, YH89GMV676, LOK3I16O7G, 59677RXH25, VH659J61ZL, 0YPR65R21J, 11E6VI8VEG, Q1RGP4UB73, 9IH82J936J, 5EF0HWI5WU, Z4B6561488, S72O3284MS, 7S82P3R43Z, 2H1576D5WG, 6P669D8HQ8, 1MBW07J51Q, RWG7BD1032, 7H443NUB2T, V5VD430YW9, F5452U54PN, C73BK97H5J, 6T6CO7R3Z5, 91D9GV0Z28, ZPS7Q5U53K, 85HKB87105, SMV71DDI4T, ETJ7Z6XBU4, 7B69B0BD62, 6RV024OAUQ
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder; Standardized Insect Venom Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911068901 followed by a unit qualifier and the quantity

Package 44911-0689-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 27, 2026.

Indications (excerpt from the label)

USES: May temporarily relieve symptoms associated with lymphatic congestion, such as: • tendency to catch colds • fluid retention • fatigue.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)