What is NDC 44911-0587?

44911-0587 is the product NDC for Joint Tone AI, Black cohosh 3 [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?

Joint Tone AI (Cimicifuga Racemosa, Lappa Major, Trifolium Pratense, Colchicum Autumnale, Dulcamara, Lycopodium Clavatum, Pulsatilla (Pratensis), Rhododendron Chrysanthum, Rhus Tox).

What is the active ingredient?

Black cohosh, Arctium lappa root, Trifolium pratense flower, Colchicum autumnale bulb, Solanum dulcamara top, Lycopodium clavatum spore, Pulsatilla pratensis whole, Rhododendron aureum leaf, Toxicodendron pubescens leaf.

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 Joint Tone AI?

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.

Joint Tone AI NDC 44911-0587 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0587Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0587Add 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
44911-0587-1	44911058701	30 mL in 1 BOTTLE, DROPPER (44911-0587-1)Marketed from Jun 21, 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): Joint Tone AI
Generic name (nonproprietary): cimicifuga racemosa, lappa major, trifolium pratense, colchicum autumnale, dulcamara, lycopodium clavatum, pulsatilla (pratensis), rhododendron chrysanthum, rhus tox
Active ingredients: Black cohosh — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLColchicum autumnale bulb — 12 [hp_X]/mLSolanum dulcamara top — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLRhododendron aureum leaf — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 21, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0587_3e2c6f05-ef33-468a-aa73-2e8e64f3a44bSPL ID 3e2c6f05-ef33-468a-aa73-2e8e64f3a44bSPL set ID bcd543aa-eb43-455e-9a73-37323f050e24UNII K73E24S6X9, 597E9BI3Z3, 4JS0838828, 993QHL78E6, KPS1B1162N, C88X29Y479, 8E272251DI, IV92NQJ73U, 6IO182RP7AUPC 0363113701357

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

N444911058701 followed by a unit qualifier and the quantity

Package 44911-0587-01. 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 Oct 4, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve pain and swelling of shoulder, arm, fingers, and small joints, and stiffness of the hands and feet.** **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 44911-0587

What is NDC 44911-0587?: 44911-0587 is the product NDC for Joint Tone AI, Black cohosh 3 [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?: Joint Tone AI (Cimicifuga Racemosa, Lappa Major, Trifolium Pratense, Colchicum Autumnale, Dulcamara, Lycopodium Clavatum, Pulsatilla (Pratensis), Rhododendron Chrysanthum, Rhus Tox).
What is the active ingredient?: Black cohosh, Arctium lappa root, Trifolium pratense flower, Colchicum autumnale bulb, Solanum dulcamara top, Lycopodium clavatum spore, Pulsatilla pratensis whole, Rhododendron aureum leaf, Toxicodendron pubescens leaf.
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 Joint Tone AI?: 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.