NDC 57955-9982-02 — Arthritis Pain and Joint Relief Actaea

🆔 Identity & classification

FDA NDC (as labeled) 57955-9982-2

Product NDC 57955-9982

11-digit billing NDC 57955998202

UNII 3FU86L9OS0, 3C18L6RJAZ, O80TY208ZW, 2HU33I03UY, T7J046YI2B, 2E32821G6I +12 more

SPL Set ID 8ecb7378-ea84-483c-ba1c-852d1ae7b90d

Established class (EPC) Calculi Dissolution Agent; Mood Stabilizer [

Mechanism of action Magnesium Ion Exchange Activity

Physiologic effect Increased Large Intestinal Motility; Inhibition Large Intestine Fluid/Electrolyte Absorption; Inhibition Small Intestine Fluid/Electrolyte Absorption

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2026-03-10

Route ORAL

Dosage form LIQUID

Substance 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 T

Why two NDCs? The FDA registers this code as 57955-9982-2 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 57955-9982-02. Same drug, same package — only the format differs.

Where does this data come from?

Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerKing Bio Inc.

Labeler code57955

First marketedMar 2026

Product typeHuman Otc Drug

Portfolio30 products on file

🔎 All NDCs from King Bio Inc.

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).

Where does this data come from?

Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is an unapproved homeopathic oral liquid containing multiple plant and mineral ingredients traditionally used in homeopathic practice for joint and arthritis-related discomfort. Homeopathic products are marketed based on homeopathic tradition rather than evaluated by the FDA for effectiveness or safety. The ingredients in this product, such as arnica, bryonia, hypericum, black cohosh, and horse chestnut, are commonly included in homeopathic formulations intended to address joint pain and inflammation, though homeopathic effectiveness has not been established through standard medical testing.

Patient education

📘 MedlinePlus patient leaflet ↗

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →

Where does this data come from?

Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

UNII XF417D3PSL
Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
UNII 1VPU26JZZ4
Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

3 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesCitric acid, Potassium sorbate, and USP purified water.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?

Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?

No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.

Why might an inactive ingredient be missing?

Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.

Can inactive ingredients matter?

Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price system	Per mL	Per package
Retail pharmacies payNADAC · weekly	Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo	No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly	No Part D plan price is available for this NDC in our data.

ℹ️

No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.

Where does this data come from?

NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Arthritis Pain and Joint Relief 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_Xthis 57955-9982-02	King	59 ml	—	—	FDA listed	—

About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.

Where does this data come from?

Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️

2026

On the market since

Mar 2026

📍

2026

Currently FDA-listed

listed with the FDA

🔒

·

No generic listed yet

brand only

ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?

Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
57955-9982-02 You're viewing this	59 mL in 1 BOTTLE, SPRAY (57955-9982-2)	2026-03-10	Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

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, Phosp 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X]/59mL; 10 [hp_X LIQUID is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand

NDC identity (package / product / labeler codes)	✓ Available
Labeler	✓ Available
Product & package description	✓ Available
Marketing category & status	✓ Available
Active ingredient / dosage form / route	✓ Available
FDA label (SPL via DailyMed)	✓ Available
Package photos	— Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured)	✓ Available
NADAC pharmacy acquisition price (CMS)	— Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data	— Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk	— Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD)	— Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.

“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?

An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.

Why is there no price listed?

The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.

Is the NDC printed on the package the same as the 11-digit billing NDC?

Yes, they identify this exact package in different formats. The FDA registers it as 57955-9982-2, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 57955-9982-02, written without dashes as 57955998202. The Identity section at the top of this page lists every form of this code.

What do the three segments of this NDC mean?

In 57955-9982-02, the first segment (57955) is the labeler code FDA assigned to King Bio Inc.; the middle segment (9982) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.

Is this package still being marketed?

Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by King Bio Inc.. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

King Bio Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.

Do I need a prescription for this product?

This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.

This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.

Where does this data come from?

Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.

🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose

🎯 Indications and Usage 40 words ▾

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.

⏱️ Dosage and Administration 46 words ▾

Directions Oral Dose Adults and Children over 12 2 sprays into mouth 3 to 6 times per day Children 6-12 1 spray into mouth 3 to 6 times per day Children under 6 Do not use in children under 6, unless directed to by a doctor

⚠️ Warnings 27 words ▾

Warnings Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.

🧪 Active Ingredient 82 words ▾

Active ingredients Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM potencies. 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. ** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″

🧪 Inactive Ingredients 10 words ▾

Inactive Ingredients Citric acid, Potassium sorbate, and USP purified water.

🎯 Purpose 123 words ▾

Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM potencies. Active ingredients Purpose † Actaea spicata........................................fatigued joints Aesculus hippocastanum.............................aching limbs Arnica montana...........................................body aches Bellis perennis...................................muscular soreness Bryonia.........................................................irritability Calcarea carbonica........................................leg cramps Calcarea fluorica.............................................backache Causticum................................................muscle aches Cimicifuga racemosa....................restless limbs, soreness Formicum acidum...........................................stiff joints Hypericum perforatum.............................joint discomfort Ledum palustre...............................aching in lower limbs Lithium carbonicum.......................aching joints, stiffness Magnesia phosphorica...................................leg cramps Phosphorus....................................................backache Phytolacca decandra.........................................stiffness Pulsatilla....................................hip and joint discomfort Rhododendron chrysanthum.....................achy shoulders Rhus tox..............................sore tendons and ligaments Ruta graveolens.........................................restlessness Salicylicum acidum..............................knee discomforts Sepia........................................stiffness, restless limbs Zincum metallicum........................................backache ** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″ † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

🔗 Related NDC lookups

🧪 All 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, Phosp NDCsSame ingredient 🏭 All King labeler NDCsLabeler code 57955 📚 All Calculi Dissolution Agent NDCsDrug class