What is NDC 43689-0015?

43689-0015 is the product NDC for Pain and Fatigue Relief, Aconitum napellus whole 30 [hp_C]/1 + 10 more ingredients tablet, listed with the FDA by The Magni Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Pain and Fatigue Relief (Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum, Lacticum Acidum, Phosphoricum Acidum, Rhus Tox, Uricum Acidum).

What is the active ingredient?

Aconitum napellus whole, Arsenic trioxide, Atropa belladonna, Coniine, Gelsemium sempervirens root, Hypericum perforatum whole, Potassium dichromate, Lactic acid, Dl-, Phosphoric acid, Toxicodendron pubescens leaf, Uric acid.

The Magni Company, NDC labeler code 43689. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pain and Fatigue Relief?

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.

Pain and Fatigue Relief NDC 43689-0015

NDC codes

FDA NDC Directory

Product NDC (as listed)43689-0015Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43689-0015Add 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
43689-0015-2	4368900150243689001502	1 BOTTLE in 1 CARTON (43689-0015-2) / 125 TABLET in 1 BOTTLE (43689-0015-1)Marketed from Jun 12, 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): Pain and Fatigue Relief
Generic name (nonproprietary): aconitum napellus, arsenicum album, belladonna, coniinum, gelsemium sempervirens, hypericum perforatum, kali bichromicum, lacticum acidum, phosphoricum acidum, rhus tox, uricum acidum
Active ingredients: Aconitum napellus whole — 30 [hp_C]/1Arsenic trioxide — 30 [hp_C]/1Atropa belladonna — 30 [hp_C]/1Coniine — 30 [hp_C]/1Gelsemium sempervirens root — 30 [hp_C]/1Hypericum perforatum whole — 3 [hp_X]/1Potassium dichromate — 30 [hp_C]/1Lactic acid, Dl- — 30 [hp_C]/1Phosphoric acid — 30 [hp_C]/1Toxicodendron pubescens leaf — 30 [hp_C]/1Uric acid — 30 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: The Magni CompanyNDC labeler code 43689
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 12, 2015
Marketing end: Apr 20, 2027
Identifiers: Product ID 43689-0015_ec83ed89-ee4e-408e-8dcf-244a762a5e9bSPL ID ec83ed89-ee4e-408e-8dcf-244a762a5e9bSPL set ID 7c689153-2002-421d-b573-76b0052550e0UNII U0NQ8555JD, S7V92P67HO, WQZ3G9PF0H, C479P32L2D, 639KR60Q1Q, XK4IUX8MNB, T4423S18FM, 3B8D35Y7S4, E4GA8884NN, 6IO182RP7A, 268B43MJ25

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

N443689001502 followed by a unit qualifier and the quantity

Package 43689-0015-02. 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 Jan 26, 2023.

Indications (excerpt from the label)

INDICATIONS: Temporarily relieves widespread aches, pains, and stiffness with fatigue

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43689-0015

What is NDC 43689-0015?: 43689-0015 is the product NDC for Pain and Fatigue Relief, Aconitum napellus whole 30 [hp_C]/1 + 10 more ingredients tablet, listed with the FDA by The Magni Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pain and Fatigue Relief (Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum, Lacticum Acidum, Phosphoricum Acidum, Rhus Tox, Uricum Acidum).
What is the active ingredient?: Aconitum napellus whole, Arsenic trioxide, Atropa belladonna, Coniine, Gelsemium sempervirens root, Hypericum perforatum whole, Potassium dichromate, Lactic acid, Dl-, Phosphoric acid, Toxicodendron pubescens leaf, Uric acid.
Who is the labeler?: The Magni Company, NDC labeler code 43689. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pain and Fatigue Relief?: 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.