Jointforce R-HP NDC 43857-0621

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0621Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0621Add 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
43857-0621-1	43857062101	30 mL in 1 BOTTLE, DROPPER (43857-0621-1)Marketed from Feb 3, 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): Jointforce R-HP
Generic name (nonproprietary): bryonia (alba), colchicum autumnale, kalmia latifolia, ledum palustre, lycopodium clavatum, rhododendron chrysanthum, rhus tox
Active ingredients: Bryonia alba root — 30 [hp_X]/mLColchicum autumnale bulb — 30 [hp_X]/mLKalmia latifolia leaf — 30 [hp_X]/mLLedum palustre twig — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLRhododendron aureum leaf — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 3, 2022
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0621_397aab3b-8560-48ae-9b21-9b380008e5b1SPL ID 397aab3b-8560-48ae-9b21-9b380008e5b1SPL set ID 9d243d5d-af08-470f-b3ec-b733bb91d1a2UNII T7J046YI2B, 993QHL78E6, 79N6542N18, 877L01IZ0P, C88X29Y479, IV92NQJ73U, 6IO182RP7AUPC 0810184340409

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

N443857062101 followed by a unit qualifier and the quantity

Package 43857-0621-01. 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 5, 2026.

Indications (excerpt from the label)

USES: For temporary relief of symptoms such as aches, pains, fever, and swelling due to inflammation of the connective tissue surrounding the joints; weak and numb feeling limbs; gouty pains in foot and painful soles.** **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)