NDC 63479-0112-01 — A12 DTX-KIDNEY APIS MELLIFICA, BERBERIS

🆔 Identity & classification

FDA NDC (as labeled) 63479-0112-1

Product NDC 63479-0112

11-digit billing NDC 63479011201

UNII 1WZA4Y92EX, 5405K23S50, 3R504894L9, 5HW39H9KDH, 5HOC10FSIC, 6D5V13045W +8 more

SPL Set ID bf52e26f-aa27-87ca-e053-2995a90a23e7

Established class (EPC) Calculi Dissolution Agent; Anti-coagulant; Standardized Insect Venom Allergenic Extract

Mechanism of action Acidifying Activity; Calcium Chelating Activity

Physiologic effect Decreased Coagulation Factor Activity; Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production

Chemical class Allergens; Bee Venoms

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 1998-10-15

Route SUBLINGUAL

Dosage form SOLUTION/ DROPS

Substance PETROSELINUM CRISPUM; SOLIDAGO VIRGAUREA FLOWERING TOP; BETULA PUBESCENS BARK; BETULA PENDULA LEAF; BEEF KIDNEY; FAGUS SYLVATICA FLOWER BUD; BERBERIS VULGARIS ROOT BARK; BOS TAURUS URINARY BLADDER; ANHYDROUS CITRIC ACID; LEMON JUICE; QUERCUS ROBUR FLOWER

Why two NDCs? The FDA registers this code as 63479-0112-1 — 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 → 63479-0112-01. 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

LabelerApex Energetics Inc.

Labeler code63479

First marketedOct 1998

Product typeHuman Otc Drug

Portfolio110 products on file

🔎 All NDCs from Apex Energetics Inc.

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 solution taken as sublingual drops. It contains multiple plant, animal, and mineral substances prepared according to homeopathic methods, including extracts of kidney and bladder tissue, various plant materials such as birch leaf and oak flower bud, and citric acid. Homeopathic products are marketed based on traditional homeopathic practices rather than clinical evidence evaluated by the FDA for safety or effectiveness. The ingredients listed have been historically used in homeopathic medicine, though their homeopathic uses are not established through standard medical research.

Patient education

📘 MedlinePlus patient leaflet ↗

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

UNII 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

2 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesalcohol (20% by volume), distilled water

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?

Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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 system	Per mL	Per 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
A12 Dtx-Kidney 2 [hp_X]/mL; 1 [hp_X]/mL; 3 [hp_X]/mL; 1 [hp_X]/mL; 7 [hp_C]/mL; 1 [hp_X]/mL; 9 [hp_X]/mLthis 63479-0112-01	Apex	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

🏛️

1998

On the market since

Oct 1998

📍

2026

Currently FDA-listed

28 years listed

🔒

·

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 NDC	Description	Marketing start	Status
63479-0112-01 You're viewing this	30 mL in 1 BOTTLE, GLASS (63479-0112-1)	1998-10-15	Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

A12 DTX-KIDNEY APIS MELLIFICA, BERBERIS VULGARIS, BETULA PUBESCENS BARK, BETULA VERRUCOSA LEAF, BOS TAURUS KIDNEY, BOS TAURUS URINARY BLADDER, CITRICUM ACIDUM, CITRUS LIMONUM, FAGUS SYLVESTRIS FLOWER BUD, NATRUM MURIATICUM, PETROSELINUM SATIVUM, QUERCUS ROBUR FLOWER BUD 2 [hp_X]/mL; 1 [hp_X]/mL; 3 [hp_X]/mL; 1 [hp_X]/mL; 7 [hp_C]/mL; 1 [hp_X]/mL; 9 [hp_X]/mL SOLUTION/ DROPS 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)	✓ 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 63479-0112-1, 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: 63479-0112-01, written without dashes as 63479011201. 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 63479-0112-01, the first segment (63479) is the labeler code FDA assigned to Apex Energetics Inc.; the middle segment (0112) 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 Apex Energetics Inc.. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

Apex Energetics 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 26 words ▾

Uses: For temporary relief of minor: urinary discomfort* headache* vertigo* water retention* backache* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

⏱️ Dosage and Administration 37 words ▾

Directions: Adults & children ages 12 years and over: Take10 drops under the tongue 2-3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

⚠️ Warnings 74 words ▾

Warnings: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if urinary discomfort, headache, vertigo, water retention, backache, or other symptoms do not improve within 7 days or are accompanied by fever.

🧪 Active Ingredient 56 words ▾

Active Ingredients Apis Mellifica 6X Berberis Vulgaris 4X 6X 9X Betula Pubescens Bark 3X Betula Verrucosa Leaf 1X Bos Taurus Kidney 7C Bos Taurus Urinary Bladder 7C Citricum Acidum 12X Citrus Limonum 3X Fagus Sylvestris Flower Bud 1X Natrum Muriaticum 9X 12X 15X Petroselinum Sativum 2X Quercus Robur Flower Bud 1X Sinusitisinum 7C Solidago Virgaurea 1X

🧪 Inactive Ingredients 8 words ▾

Inactive Ingredients alcohol (20% by volume), distilled water

🎯 Purpose 26 words ▾

Uses: For temporary relief of minor: urinary discomfort* headache* vertigo* water retention* backache* *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 ↗

🔗 Related NDC lookups

🧪 All Apis Mellifica, Berberis Vulgaris, Betula Pubescens Bark, Betula Verrucosa Leaf, Bos Taurus Kidney, Bos Taurus Urinary Bladder, Citricum Acidum, Citrus Limonum, Fagus Sylvestris Flower Bud, Natrum Muriaticum, Petroselinum Sativum, Quercus Robur Flower Bud NDCsSame ingredient 🏭 All Apex labeler NDCsLabeler code 63479 📚 All Anti-coagulant NDCsDrug class