What is NDC 44911-0624?

44911-0624 is the product NDC for Back and Leg HP, Aconitum napellus whole 30 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Back and Leg HP (Aconitum Napellus, Aesculus Hippocastanum, Colocynthis, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Plumbum Metallicum, Rhus Tox, Arnica Montana).

What is the active ingredient?

Aconitum napellus whole, Horse chestnut, Citrullus colocynthis fruit pulp, Pseudognaphalium obtusifolium whole, Hypericum perforatum whole, Magnesium phosphate, Dibasic trihydrate, Lead, Toxicodendron pubescens leaf, Arnica montana whole.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Back and Leg HP?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Back and Leg HP NDC 44911-0624 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0624Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0624Add 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
44911-0624-1	4491106240144911062401	30 mL in 1 BOTTLE, DROPPER (44911-0624-1)Marketed from May 27, 2021

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): Back and Leg HP
Generic name (nonproprietary): aconitum napellus, aesculus hippocastanum, colocynthis, gnaphalium polycephalum, hypericum perforatum, magnesia phosphorica, plumbum metallicum, rhus tox, arnica montana
Active ingredients: Aconitum napellus whole — 30 [hp_X]/mLHorse chestnut — 30 [hp_X]/mLCitrullus colocynthis fruit pulp — 30 [hp_X]/mLPseudognaphalium obtusifolium whole — 30 [hp_X]/mLHypericum perforatum whole — 30 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 30 [hp_X]/mLLead — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLArnica montana whole — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 44911-0624_7561e824-ceb3-4d2c-8090-748a858daf10SPL ID 7561e824-ceb3-4d2c-8090-748a858daf10SPL set ID 45f8cdd2-d518-453a-8aa4-a0cb6b4e6eb0UNII U0NQ8555JD, 3C18L6RJAZ, 23H32AOH17, 36XQ854NWW, XK4IUX8MNB, HF539G9L3Q, 2P299V784P, 6IO182RP7A, O80TY208ZWUPC 0363113700510
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N444911062401 followed by a unit qualifier and the quantity

Package 44911-0624-01. 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 Nov 30, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of sharp pain in lower back and down the back of the legs and bursitis.** **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)

About NDC 44911-0624

What is NDC 44911-0624?: 44911-0624 is the product NDC for Back and Leg HP, Aconitum napellus whole 30 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Back and Leg HP (Aconitum Napellus, Aesculus Hippocastanum, Colocynthis, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Plumbum Metallicum, Rhus Tox, Arnica Montana).
What is the active ingredient?: Aconitum napellus whole, Horse chestnut, Citrullus colocynthis fruit pulp, Pseudognaphalium obtusifolium whole, Hypericum perforatum whole, Magnesium phosphate, Dibasic trihydrate, Lead, Toxicodendron pubescens leaf, Arnica montana whole.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Back and Leg HP?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.