Jointox BB NDC 44911-0642

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0642Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0642Add 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
44911-0642-1	44911064201	60 mL in 1 BOTTLE, DROPPER (44911-0642-1)Marketed from May 26, 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): Jointox BB
Generic name (nonproprietary): baptisia tinctoria, echinacea (angustifolia), hydrastis canadensis, borrelia burgdorferi nosode, babesia microti, ehrlichia nosode (canine), hepatitis b nosode, meningococcus nosode, arsenicum album, bryonia (alba), chelidonium majus, colchicum autumnale, kalmia latifolia, ledum palustre, lycopodium clavatum, phosphorus, rhus tox
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLBorrelia burgdorferi — 12 [hp_X]/mLBabesia microti — 20 [hp_X]/mLEhrlichia canis — 20 [hp_X]/mLNeisseria meningitidis — 30 [hp_X]/mLHepatitis b virus — 30 [hp_X]/mLArsenic trioxide — 30 [hp_C]/mLBryonia alba root — 30 [hp_C]/mLChelidonium majus whole — 30 [hp_C]/mLColchicum autumnale bulb — 30 [hp_C]/mLKalmia latifolia leaf — 30 [hp_C]/mLLedum palustre twig — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLToxicodendron pubescens leaf — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: May 26, 2021
Marketing end: Dec 19, 2028
Identifiers: Product ID 44911-0642_07617cf8-dc45-4166-9256-db5038717f5dSPL ID 07617cf8-dc45-4166-9256-db5038717f5dSPL set ID 4b66fc44-6953-4463-a085-a11beb612cadUNII 5EF0HWI5WU, VB06AV5US8, ZW3Z11D0JV, 0J8NV9V5Q8, 1948X6KEG3, 970Y8T1JZY, V3TP2MD7F3, 77H9EM77P7, S7V92P67HO, T7J046YI2B, 7E889U5RNN, 993QHL78E6, 79N6542N18, 877L01IZ0P, C88X29Y479, 27YLU75U4W, 6IO182RP7AUPC 0363113700848

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

N444911064201 followed by a unit qualifier and the quantity

Package 44911-0642-01. 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 May 19, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve rash, fatigue, insomnia, weakness in limbs, and joint and muscle discomfort** **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)