Leg and Back Pain Relief NDC 43689-0013

NDC codes

FDA NDC Directory

Product NDC (as listed)43689-0013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43689-0013Add 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
43689-0013-2	43689001302	1 BOTTLE in 1 CARTON (43689-0013-2) / 125 TABLET in 1 BOTTLE (43689-0013-1)Marketed from Jun 11, 2015

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): Leg and Back Pain Relief
Generic name (nonproprietary): capsicum annuum, colocynthis, gnaphalium polycephalum, magnesia phosphorica
Active ingredients: Capsicum — 6 [hp_X]/1Citrullus colocynthis fruit pulp — 6 [hp_X]/1Pseudognaphalium obtusifolium — 6 [hp_X]/1Magnesium phosphate, Dibasic trihydrate — 6 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: The Magni Company
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 11, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)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)Plant Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43689-0013_bc3ebce9-dde9-4bde-8568-878ab1c5be26SPL ID bc3ebce9-dde9-4bde-8568-878ab1c5be26SPL set ID ef30c7cf-6da0-424d-8737-c968436768fdUNII 00UK7646FG, 23H32AOH17, 36XQ854NWW, HF539G9L3Q
Pharmacologic class: Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; 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

N443689001302 followed by a unit qualifier and the quantity

Package 43689-0013-02. 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 Apr 22, 2026.

Indications (excerpt from the label)

USES: For the temporary relief of minor aches and pains in the lower back, buttocks, and legs

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)