Arnicare Leg Cramps NDC 0220-9079

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9079Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9079Add 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
0220-9079-04	00220907904	1 BLISTER PACK in 1 CARTON (0220-9079-04) / 60 TABLET in 1 BLISTER PACKMarketed from Sep 11, 2023
0220-9079-29	00220907929	1 BLISTER PACK in 1 CARTON (0220-9079-29) / 120 TABLET in 1 BLISTER PACKMarketed from Nov 7, 2023
0220-9079-92	00220907992	5 BLISTER PACK in 1 CARTON (0220-9079-92) / 20 TABLET in 1 BLISTER PACKMarketed from Jul 20, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Arnicare Leg Cramps
Generic name (nonproprietary): arnica montana whole, copper, magnesium phosphate, dibasic trihydrate, strychnos nux-vomica seed, passiflora incarnata top, claviceps purpurea sclerotium
Active ingredients: Passiflora incarnata top — 3 [hp_X]/1Copper — 4 [hp_C]/1Arnica montana — 6 [hp_C]/1Magnesium phosphate, Dibasic trihydrate — 6 [hp_C]/1Strychnos nux-vomica seed — 6 [hp_C]/1Claviceps purpurea sclerotium — 9 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: Laboratoires Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 11, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibit Ovum Fertilization (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)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 0220-9079_570fbc3a-1c54-e0f6-e063-6394a90a6d25SPL ID 570fbc3a-1c54-e0f6-e063-6394a90a6d25SPL set ID 051a4e17-c665-ec4d-e063-6294a90aabe6UNII CLF5YFS11O, 789U1901C5, O80TY208ZW, HF539G9L3Q, 269XH13919, 01G9XEA93N
Pharmacologic class: Calculi Dissolution Agent; Copper-containing Intrauterine Device; Non-Standardized Plant Allergenic Extract; 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

N400220907904 followed by a unit qualifier and the quantity

Package 00220-9079-04. 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 Jul 20, 2026.

Indications (excerpt from the label)

Uses* temporarily relieves nighttime cramps in legs, thighs, calves, feet, and toes with accompanying occasional disrupted sleep

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)