What is NDC 57955-9982?

57955-9982 is the product NDC for Arthritis Pain and Joint Relief, Actaea spicata root 10 [hp_X]/59mL + 22 more ingredients liquid, listed with the FDA by King Bio Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Arthritis Pain and Joint Relief (Actaea spicata, Aesculus hippocastanum, Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Calcarea fluorica, Causticum, Cimicifuga racemosa, Formicum acidum, Hypericum perforatum, Ledum palustre, Lithium carbonicum, Magnesia phosphorica, Phosphorus, Phytolacca decandra, Pulsatilla, Rhododendron chrysanthum, Rhus tox, Ruta graveolens, Salicylicum acidum, Sepia and Zincum metallicum.).

What is the active ingredient?

Actaea spicata root, Horse chestnut, Arnica montana whole, Bellis perennis whole, Bryonia alba root, Oyster shell calcium carbonate, Crude, Calcium fluoride, Causticum, Black cohosh, Formic acid, Hypericum perforatum whole, Rhododendron tomentosum leafy twig, Lithium carbonate, Magnesium phosphate, Dibasic trihydrate, Phosphorus, Phytolacca americana root, Pulsatilla vulgaris whole, Rhododendron aureum leaf, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Salicylic acid, Sepia officinalis juice, Zinc.

King Bio Inc., NDC labeler code 57955. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Arthritis Pain and Joint Relief?

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.

Arthritis Pain and Joint Relief NDC 57955-9982

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9982Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9982Add 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
57955-9982-2	5795599820257955998202	59 mL in 1 BOTTLE, SPRAY (57955-9982-2)Marketed from Mar 10, 2026

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): Arthritis Pain and Joint Relief
Generic name (nonproprietary): actaea spicata, aesculus hippocastanum, arnica montana, bellis perennis, bryonia, calcarea carbonica, calcarea fluorica, causticum, cimicifuga racemosa, formicum acidum, hypericum perforatum, ledum palustre, lithium carbonicum, magnesia phosphorica, phosphorus, phytolacca decandra, pulsatilla, rhododendron chrysanthum, rhus tox, ruta graveolens, salicylicum acidum, sepia and zincum metallicum.
Active ingredients: Actaea spicata root — 10 [hp_X]/59mLHorse chestnut — 10 [hp_X]/59mLArnica montana whole — 10 [hp_X]/59mLBellis perennis whole — 10 [hp_X]/59mLBryonia alba root — 10 [hp_X]/59mLOyster shell calcium carbonate, Crude — 10 [hp_X]/59mLCalcium fluoride — 10 [hp_X]/59mLCausticum — 10 [hp_X]/59mLBlack cohosh — 10 [hp_X]/59mLFormic acid — 10 [hp_X]/59mLHypericum perforatum whole — 10 [hp_X]/59mLRhododendron tomentosum leafy twig — 10 [hp_X]/59mLLithium carbonate — 10 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/59mLPhosphorus — 10 [hp_X]/59mLPhytolacca americana root — 10 [hp_X]/59mLPulsatilla vulgaris whole — 10 [hp_X]/59mLRhododendron aureum leaf — 10 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLRuta graveolens flowering top — 10 [hp_X]/59mLSalicylic acid — 10 [hp_X]/59mLSepia officinalis juice — 10 [hp_X]/59mLZinc — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.NDC labeler code 57955
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 10, 2026
Listing expires: Dec 31, 2027
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 57955-9982_4e81f0ce-1c4c-4ec6-9c76-1251b1589f77SPL ID 4e81f0ce-1c4c-4ec6-9c76-1251b1589f77SPL set ID 8ecb7378-ea84-483c-ba1c-852d1ae7b90dUNII 3FU86L9OS0, 3C18L6RJAZ, O80TY208ZW, 2HU33I03UY, T7J046YI2B, 2E32821G6I, O3B55K4YKI, DD5FO1WKFU, K73E24S6X9, 0YIW783RG1, XK4IUX8MNB, 877L01IZ0P, 2BMD2GNA4V, HF539G9L3Q, 27YLU75U4W, 11E6VI8VEG, I76KB35JEV, IV92NQJ73U, 6IO182RP7A, N94C2U587S, O414PZ4LPZ, QDL83WN8C2, J41CSQ7QDS
Pharmacologic class: Calculi Dissolution Agent; Mood Stabilizer; 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

N457955998202 followed by a unit qualifier and the quantity

Package 57955-9982-02. 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 2, 2026.

Indications (excerpt from the label)

Uses † For temporary relief of: backache leg cramps stiff swollen joints irritability sore tendons and ligaments body aches hip and knee discomforts fatigue restless limbs † 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 57955-9982

What is NDC 57955-9982?: 57955-9982 is the product NDC for Arthritis Pain and Joint Relief, Actaea spicata root 10 [hp_X]/59mL + 22 more ingredients liquid, listed with the FDA by King Bio Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Arthritis Pain and Joint Relief (Actaea spicata, Aesculus hippocastanum, Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Calcarea fluorica, Causticum, Cimicifuga racemosa, Formicum acidum, Hypericum perforatum, Ledum palustre, Lithium carbonicum, Magnesia phosphorica, Phosphorus, Phytolacca decandra, Pulsatilla, Rhododendron chrysanthum, Rhus tox, Ruta graveolens, Salicylicum acidum, Sepia and Zincum metallicum.).
What is the active ingredient?: Actaea spicata root, Horse chestnut, Arnica montana whole, Bellis perennis whole, Bryonia alba root, Oyster shell calcium carbonate, Crude, Calcium fluoride, Causticum, Black cohosh, Formic acid, Hypericum perforatum whole, Rhododendron tomentosum leafy twig, Lithium carbonate, Magnesium phosphate, Dibasic trihydrate, Phosphorus, Phytolacca americana root, Pulsatilla vulgaris whole, Rhododendron aureum leaf, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Salicylic acid, Sepia officinalis juice, Zinc.
Who is the labeler?: King Bio Inc., NDC labeler code 57955. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Arthritis Pain and Joint Relief?: 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.