Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Back, Muscle and Joint Relief NDC 57955-9984
Horse chestnut 10 [hp_X]/59mL + 17 more ingredients · Liquid · Oral · King Bio Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 57955-9984-2 | 5795599840257955998402 | 59 mL in 1 BOTTLE, SPRAY (57955-9984-2)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)
- Back, Muscle and Joint Relief
- Generic name (nonproprietary)
- aesculus hippocastanum, arnica montana, bellis perennis, bryonia, calcarea carbonica, calcarea fluorica, cimicifuga racemosa, cobaltum metallicum, gnaphalium polycephalum, hypericum perforatum, kali carbonicum, kali phosphoricum, magnesia phosphorica, oxalicum acidum, phosphorus, rhus tox, ruta graveolens, and zincum metallicum.
- Active ingredients
- Horse 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]/59mLBlack cohosh — 10 [hp_X]/59mLCobalt — 10 [hp_X]/59mLPseudognaphalium obtusifolium whole — 10 [hp_X]/59mLHypericum perforatum whole — 10 [hp_X]/59mLPotassium carbonate — 10 [hp_X]/59mLDibasic potassium phosphate — 10 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/59mLOxalic acid dihydrate — 10 [hp_X]/59mLPhosphorus — 10 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLRuta graveolens flowering top — 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
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)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 57955-9984_6fa9c0ec-4ddd-4a8a-8175-e27b8e209718SPL ID 6fa9c0ec-4ddd-4a8a-8175-e27b8e209718SPL set ID c6e50f93-bc45-4755-8ab0-dbe0d9987fcaUNII 3C18L6RJAZ, O80TY208ZW, 2HU33I03UY, T7J046YI2B, 2E32821G6I, O3B55K4YKI, K73E24S6X9, 3G0H8C9362, 36XQ854NWW, XK4IUX8MNB, BQN1B9B9HA, CI71S98N1Z, HF539G9L3Q, 0K2L2IJ59O, 27YLU75U4W, 6IO182RP7A, N94C2U587S, J41CSQ7QDS
- Pharmacologic class
- Calculi Dissolution Agent; Osmotic Laxative; Standardized Chemical Allergen
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
N457955998402followed by a unit qualifier and the quantityPackage 57955-9984-02. 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 .
Indications (excerpt from the label)
Uses † For temporary relief of: back discomforts muscle tension and cramps weakness and fatigue joint stiffness body aches soreness restlessness tired legs and feet † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.
Excerpt only. Read the full label for complete information.
About NDC 57955-9984
- What is NDC 57955-9984?
- 57955-9984 is the product NDC for Back, Muscle and Joint Relief, Horse chestnut 10 [hp_X]/59mL + 17 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?
- Back, Muscle and Joint Relief (Aesculus hippocastanum, Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Calcarea fluorica, Cimicifuga racemosa, Cobaltum metallicum, Gnaphalium polycephalum, Hypericum perforatum, Kali carbonicum, Kali phosphoricum, Magnesia phosphorica, Oxalicum acidum, Phosphorus, Rhus tox, Ruta graveolens, and Zincum metallicum.).
- What is the active ingredient?
- Horse chestnut, Arnica montana whole, Bellis perennis whole, Bryonia alba root, Oyster shell calcium carbonate, Crude, Calcium fluoride, Black cohosh, Cobalt, Pseudognaphalium obtusifolium whole, Hypericum perforatum whole, Potassium carbonate, Dibasic potassium phosphate, Magnesium phosphate, Dibasic trihydrate, Oxalic acid dihydrate, Phosphorus, Toxicodendron pubescens leaf, Ruta graveolens flowering top, 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 Back, Muscle 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.