Mitochondria PRO NDC 44911-0703

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0703Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0703Add 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
44911-0703-1	44911070301	30 mL in 1 BOTTLE, DROPPER (44911-0703-1)Marketed from Dec 28, 2023

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): Mitochondria PRO
Generic name (nonproprietary): aralia quinquefolia, arnica montana, adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, ascorbicum acidum, alpha-lipoicum acidum, calcarea carbonica, citricum acidum, cuprum metallicum, cysteinum, ferrum metallicum, iodium, levothyroxinum, magnesium gluconicum dihydricum, malicum acidum, manganum aceticum, nadidum, natrum pyruvicum, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, selenium metallicum, sulphur, thiaminum hydrochloricum, ubidecarenonum, zincum metallicum,
Active ingredients: American ginseng — 6 [hp_X]/mLArnica montana whole — 6 [hp_X]/mLAdenosine triphosphate disodium — 12 [hp_X]/mLOxogluric acid — 12 [hp_X]/mLAscorbic acid — 12 [hp_X]/mLAlpha lipoic acid — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLAnhydrous citric acid — 12 [hp_X]/mLCopper — 12 [hp_X]/mLCysteine — 12 [hp_X]/mLIron — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLevothyroxine — 12 [hp_X]/mLMagnesium gluconate — 12 [hp_X]/mLMalic acid — 12 [hp_X]/mLManganese acetate tetrahydrate — 12 [hp_X]/mLNadide — 12 [hp_X]/mLSodium pyruvate — 12 [hp_X]/mLNiacinamide — 12 [hp_X]/mLPyridoxine hydrochloride — 12 [hp_X]/mLRiboflavin — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLThiamine hydrochloride — 12 [hp_X]/mLUbidecarenone — 12 [hp_X]/mLZinc — 12 [hp_X]/mLAconitic acid, (Z)- — 16 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLCinchona officinalis bark — 30 [hp_X]/mLConium maculatum flowering top — 30 [hp_X]/mLGelsemium sempervirens root — 30 [hp_X]/mLMercurius solubilis — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mLBarium oxalosuccinate — 35 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 28, 2023
Marketing end: May 8, 2029
Other FDA classes: Acidifying Activity (Mechanism)Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Calcium Chelating Activity (Mechanism)Copper (Chemical structure)Decreased Coagulation Factor Activity (Physiologic effect)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)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Thyroxine (Chemical structure)Vitamin B 6 (Chemical/Ingredient)
Identifiers: Product ID 44911-0703_2fdabc0d-c95d-4d2d-b132-55ee5a50f275SPL ID 2fdabc0d-c95d-4d2d-b132-55ee5a50f275SPL set ID 8c3e961d-bc33-40cd-a282-a4fe5aa3f0adUNII 8W75VCV53Q, O80TY208ZW, 5L51B4DR1G, 8ID597Z82X, PQ6CK8PD0R, 73Y7P0K73Y, 2E32821G6I, XF417D3PSL, 789U1901C5, K848JZ4886, E1UOL152H7, 9679TC07X4, Q51BO43MG4, T42NAD2KHC, 817L1N4CKP, 9TO51D176N, 0U46U6E8UK, POD38AIF08, 25X51I8RD4, 68Y4CF58BV, TLM2976OFR, H6241UJ22B, 70FD1KFU70, M572600E5P, EJ27X76M46, J41CSQ7QDS, OF5471ZHRR, S7V92P67HO, T7J046YI2B, S003A158SB, Q28R5GF371, 639KR60Q1Q, 324Y4038G2, ETJ7Z6XBU4, L7A49804ZQUPC 0363113701869
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Copper-containing Intrauterine Device; Osmotic Laxative; Paramagnetic Contrast Agent; Vitamin B6 Analog; Vitamin C; l-Thyroxine

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

N444911070301 followed by a unit qualifier and the quantity

Package 44911-0703-01. 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 Oct 6, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve fatigue, weakness, loss of smell, and brain fog.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)