Arnica Plus DROPS NDC 66492-245

NDC codes

FDA NDC Directory

Product NDC (as listed)66492-245Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66492-0245Add 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
66492-245-02	66492024502	58.5 mL in 1 BOTTLE, DROPPER (66492-245-02)Marketed from Jan 1, 2000

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Arnica Plus DROPS
Generic name (nonproprietary): aconitum napellus, arnica montana, chamomilla, hypericum perforatum, ruta graveolens, symphytum officinale, belladonna, colocynthis, rhus tox, ferrum phos, magnesium phos.
Active ingredients: Aconitum napellus — 3 [hp_X]/mLArnica montana — 3 [hp_X]/mLMatricaria recutita — 3 [hp_X]/mLHypericum perforatum — 3 [hp_X]/mLRuta graveolens flowering top — 3 [hp_X]/mLComfrey root — 3 [hp_X]/mLAtropa belladonna — 4 [hp_X]/mLCitrullus colocynthis fruit pulp — 4 [hp_X]/mLToxicodendron pubescens leaf — 6 [hp_X]/mLFerrosoferric phosphate — 8 [hp_X]/mLMagnesium phosphate, Dibasic — 8 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2000
Listing expires: Dec 31, 2026
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 66492-245_d449bc17-6367-d085-e053-2995a90a2548SPL ID d449bc17-6367-d085-e053-2995a90a2548SPL set ID 54402c83-02bd-434e-a27e-b55b3fedcfc5UNII U0NQ8555JD, O80TY208ZW, G0R4UBI2ZZ, XK4IUX8MNB, N94C2U587S, M9VVZ08EKQ, WQZ3G9PF0H, 23H32AOH17, 6IO182RP7A, 91GQH8I5F7, A1Y870209ZUPC 0366492245023
Pharmacologic class: Calculi Dissolution Agent; 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

N466492024502 followed by a unit qualifier and the quantity

Package 66492-0245-02. 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 Dec 29, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves pain and inflammation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)