What is NDC 50845-0273?

50845-0273 is the product NDC for Joint plus Tendon, Aconitum napellus whole 200 [hp_C]/mL + 7 more ingredients spray, listed with the FDA by Liddell Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Joint plus Tendon (Aconitum Napellus, Apis Mellifica, Arnica Montana, Cartilago Suis, Hydrastis Canadensis, Hypericum Perforatum, Rhus Tox, Thuja Occidentalis).

What is the active ingredient?

Aconitum napellus whole, Apis mellifera, Arnica montana whole, Sus scrofa cartilage, Goldenseal, Hypericum perforatum whole, Toxicodendron pubescens leaf, Thuja occidentalis leafy twig.

Liddell Laboratories, Inc., NDC labeler code 50845. 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 plus Tendon?

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 plus Tendon NDC 50845-0273 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0273Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0273Add 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
50845-0273-1	5084502730150845027301	30 mL in 1 BOTTLE, SPRAY (50845-0273-1)Marketed from Jun 20, 2022

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 plus Tendon
Generic name (nonproprietary): aconitum napellus, apis mellifica, arnica montana, cartilago suis, hydrastis canadensis, hypericum perforatum, rhus tox, thuja occidentalis
Active ingredients: Aconitum napellus whole — 200 [hp_C]/mLApis mellifera — 200 [hp_C]/mLArnica montana whole — 200 [hp_C]/mLSus scrofa cartilage — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLHypericum perforatum whole — 200 [hp_C]/mLToxicodendron pubescens leaf — 200 [hp_C]/mLThuja occidentalis leafy twig — 200 [hp_C]/mL
Dosage form: Spray
Route: Oral
Labeler: Liddell Laboratories, Inc.NDC labeler code 50845
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 20, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 50845-0273_4b37fd54-ae68-4a07-816b-6fe304afe2e6SPL ID 4b37fd54-ae68-4a07-816b-6fe304afe2e6SPL set ID 64465f12-f50e-46ef-bb82-9b10b18cfa24UNII U0NQ8555JD, 7S82P3R43Z, O80TY208ZW, 73ECW5WG2F, ZW3Z11D0JV, XK4IUX8MNB, 6IO182RP7A, 1NT28V9397UPC 0363113007961
Pharmacologic class: 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

N450845027301 followed by a unit qualifier and the quantity

Package 50845-0273-01. 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 4, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily ease discomfort associated with inflammation of joints, tendons and nerves.** **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 50845-0273

What is NDC 50845-0273?: 50845-0273 is the product NDC for Joint plus Tendon, Aconitum napellus whole 200 [hp_C]/mL + 7 more ingredients spray, listed with the FDA by Liddell Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Joint plus Tendon (Aconitum Napellus, Apis Mellifica, Arnica Montana, Cartilago Suis, Hydrastis Canadensis, Hypericum Perforatum, Rhus Tox, Thuja Occidentalis).
What is the active ingredient?: Aconitum napellus whole, Apis mellifera, Arnica montana whole, Sus scrofa cartilage, Goldenseal, Hypericum perforatum whole, Toxicodendron pubescens leaf, Thuja occidentalis leafy twig.
Who is the labeler?: Liddell Laboratories, Inc., NDC labeler code 50845. 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 plus Tendon?: 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.