Muscle Cramp Pain Reliever NDC 43689-0022

NDC codes

FDA NDC Directory

Product NDC (as listed)43689-0022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43689-0022Add 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
43689-0022-2	43689002202	1 BOTTLE in 1 CARTON (43689-0022-2) / 125 TABLET in 1 BOTTLE (43689-0022-1)Marketed from Sep 18, 2019

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): Muscle Cramp Pain Reliever
Generic name (nonproprietary): causticum, colocynthis, cuprum metallicum, magnesia phosphorica, phytolacca decandra, rhus tox, stannum metallicum, veratrum album
Active ingredients: Causticum — 12 [hp_X]/1Citrullus colocynthis fruit pulp — 12 [hp_X]/1Copper — 12 [hp_X]/1Magnesium phosphate, Dibasic trihydrate — 12 [hp_X]/1Phytolacca americana root — 12 [hp_X]/1Toxicodendron pubescens leaf — 12 [hp_X]/1Tin — 12 [hp_X]/1Veratrum album root — 12 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: The Magni Company
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 18, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (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)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43689-0022_b7218efa-ddaa-4879-998f-4fd35196c21cSPL ID b7218efa-ddaa-4879-998f-4fd35196c21cSPL set ID e8d70c35-3ed6-479a-8213-b2fb3499a32aUNII DD5FO1WKFU, 23H32AOH17, 789U1901C5, HF539G9L3Q, 11E6VI8VEG, 6IO182RP7A, 387GMG9FH5, QNS6W5US1Z
Pharmacologic class: Calculi Dissolution Agent; Copper-containing Intrauterine Device; 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

N443689002202 followed by a unit qualifier and the quantity

Package 43689-0022-02. 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 Nov 5, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, hips and back.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)