What is NDC 57955-9979?

57955-9979 is the product NDC for Advanced Arnica Plus, Arnica montana whole 10 [hp_X]/59mL + 9 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?

Advanced Arnica Plus (Arnica montana, Arnica rad, Bellis perennis, Bryonia, Hypericum perforatum, Lithium carbonicum, Magnesia phosphorica, Phytolacca decandra, Rhus tox, and Ruta graveolens.).

What is the active ingredient?

Arnica montana whole, Arnica montana root, Bellis perennis whole, Bryonia alba root, Hypericum perforatum whole, Lithium carbonate, Magnesium phosphate, Dibasic trihydrate, Phytolacca americana root, Toxicodendron pubescens leaf, Ruta graveolens flowering top.

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 Advanced Arnica Plus?

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.

Advanced Arnica Plus NDC 57955-9979

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9979Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9979Add 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
57955-9979-2	5795599790257955997902	59 mL in 1 BOTTLE, SPRAY (57955-9979-2)Marketed from Mar 15, 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): Advanced Arnica Plus
Generic name (nonproprietary): arnica montana, arnica rad, bellis perennis, bryonia, hypericum perforatum, lithium carbonicum, magnesia phosphorica, phytolacca decandra, rhus tox, and ruta graveolens.
Active ingredients: Arnica montana whole — 10 [hp_X]/59mLArnica montana root — 10 [hp_X]/59mLBellis perennis whole — 10 [hp_X]/59mLBryonia alba root — 10 [hp_X]/59mLHypericum perforatum whole — 10 [hp_X]/59mLLithium carbonate — 10 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/59mLPhytolacca americana root — 10 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLRuta graveolens flowering top — 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 15, 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 57955-9979_c9f3c66e-e00f-4e62-beb4-5f73c663a9d0SPL ID c9f3c66e-e00f-4e62-beb4-5f73c663a9d0SPL set ID 8f1bac20-8403-4a15-bc29-f3bb1fa3c60dUNII O80TY208ZW, MUE8Y11327, 2HU33I03UY, T7J046YI2B, XK4IUX8MNB, 2BMD2GNA4V, HF539G9L3Q, 11E6VI8VEG, 6IO182RP7A, N94C2U587S
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

N457955997902 followed by a unit qualifier and the quantity

Package 57955-9979-02. 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 4, 2026.

Indications (excerpt from the label)

Uses † temporarily relief of: pain or stiffness in muscles or joints bruising and discoloration body aches inflammation soreness after exercise † 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 57955-9979

What is NDC 57955-9979?: 57955-9979 is the product NDC for Advanced Arnica Plus, Arnica montana whole 10 [hp_X]/59mL + 9 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?: Advanced Arnica Plus (Arnica montana, Arnica rad, Bellis perennis, Bryonia, Hypericum perforatum, Lithium carbonicum, Magnesia phosphorica, Phytolacca decandra, Rhus tox, and Ruta graveolens.).
What is the active ingredient?: Arnica montana whole, Arnica montana root, Bellis perennis whole, Bryonia alba root, Hypericum perforatum whole, Lithium carbonate, Magnesium phosphate, Dibasic trihydrate, Phytolacca americana root, Toxicodendron pubescens leaf, Ruta graveolens flowering top.
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 Advanced Arnica Plus?: 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.