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Mitochondria Pro 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, 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL Liquid, 30 mL — NDC 44911-0903-01 package photo

Mitochondria Pro 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, 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL Liquid, 30 mL

by Energique, Inc. · 30 mL in 1 BOTTLE, DROPPER (44911-0903-1)
NDC 44911-0903-01
🏷️ FDA NDC (as labeled) 44911-0903-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 44911-0903-1
Product NDC 44911-0903
11-digit billing NDC 44911090301
UNII 8W75VCV53Q, O80TY208ZW, 5L51B4DR1G, 8ID597Z82X, PQ6CK8PD0R, 73Y7P0K73Y +12 more
UPC 0363113701869
SPL Set ID 2f365207-b730-428d-9465-8853e86e79ff
Established class (EPC) Vitamin C; Calculi Dissolution Agent; Anti-coagulant; Copper-containing Intrauterine Device; l-Thyroxine
Mechanism of action Acidifying Activity; Calcium Chelating Activity
Physiologic effect Decreased Coagulation Factor Activity; Decreased Embryonic Implantation; Decreased Sperm Motility; Inhibit Ovum Fertilization
Chemical class Ascorbic Acid; Copper; Thyroxine
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-18
Route ORAL
Dosage form LIQUID
Substance AMERICAN GINSENG; ARNICA MONTANA WHOLE; ADENOSINE TRIPHOSPHATE DISODIUM; OXOGLURIC ACID; ASCORBIC ACID; ALPHA LIPOIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ANHYDROUS CITRIC ACID; COPPER; CYSTEINE; IRON; IODINE; LEVOTHYROXINE; MAGNESIUM GLUCONATE; MA
Why two NDCs? The FDA registers this code as 44911-0903-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 44911-0903-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerEnergique, Inc.
Labeler code44911
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio349 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is an unapproved homeopathic liquid taken by mouth that contains multiple plant extracts, minerals, and other substances. Homeopathic practitioners traditionally use ingredients in this product for purposes such as supporting energy production, circulation, and immune function, though homeopathic products are not evaluated by the FDA for effectiveness. The formulation includes arnica montana and bryonia alba, commonly selected in homeopathic practice for musculoskeletal concerns, alongside various vitamins and mineral salts. Homeopathic products are marketed based on traditional use rather than scientific evidence of safety or effectiveness.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Mitochondria Pro 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mLthis 44911-0903-01 Energique, 30 ml — — FDA listed —
Mitochondria PRO 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL 44911-0703-01 Energique, 30 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2026
On the market since
Feb 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
44911-0903-01 You're viewing this 30 mL in 1 BOTTLE, DROPPER (44911-0903-1) 2026-02-18 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Mitochondria Pro 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, 6 [hp_X]/mL; 6 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL LIQUID is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 44911-0903-1, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 44911-0903-01, written without dashes as 44911090301. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 44911-0903-01, the first segment (44911) is the labeler code FDA assigned to Energique, Inc.; the middle segment (0903) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Energique, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Energique, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 25 words ▾

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.

⏱️ Dosage and Administration 46 words ▾

DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

⚠️ Warnings 49 words ▾

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

🧪 Active Ingredient 105 words ▾

ACTIVE INGREDIENTS: (in each drop) 2.86% of Aralia Quinquefolia 6X, Arnica Montana 6X; Alpha-Ketoglutaricum Acidum 12X, Alpha-Lipoicum Acidum 12X, Ascorbicum Acidum 12X, Adenosinum Triphosphoricum Dinatrum 12X, Calcarea Carbonica 12X, Citricum Acidum 12X, Cuprum Metallicum 12X, Cysteinum 12X, Ferrum Metallicum 12X, Iodium 12X, Levothyroxinum 12X, Magnesium Gluconicum Dihydricum 12X, Malicum Acidum 12X, Manganum Aceticum 12X, Nadidum 12X, Natrum Pyruvicum 12X, Nicotinamidum 12X, Pyridoxinum Hydrochloricum 12X, Riboflavinum 12X, Selenium Metallicum 12X, Sulphur 12X, Thiaminum Hydrochloricum 12X, Ubidecarenonum 12X, Zincum Metallicum 12X; Aconiticum Acidum, Cis- 30X; Arsenicum Album 30X, Bryonia 30X, Cinchona Officinalis 30X, Conium Maculatum 30X, Gelsemium Sempervirens 30X, Mercurius Solubilis 30X, Silicea 30X; Barium Oxalsuccinicum 35C.

🧪 Inactive Ingredients 6 words ▾

INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.

🎯 Purpose 25 words ▾

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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 44911-0902-01 · Energique, 44911-0904-01 · Energique, →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.