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G03 TEST-MET ADENOSINE TRIPHOSPHATE, AMMONIUM CHLORIDE, APIS MELLIFERA, BAPTISIA TINCTORIA ROOT, CALCIUM FLUORIDE, CAMPHOR (NATURAL), CITRULLUS COLOCYNTHIS FRUIT PULP, SEQUOIA SEMPERVIRENS BARK, SPONGIA OFFICINALIS SKELETON, ROASTED, TESTOSTERONE 7 [hp_C]/mL; 1 [hp_Q]/mL; 2 [hp_Q]/mL; 12 [hp_X]/mL; 1 [hp_X]/mL; 7 [hp_C]/mL; 3 [hp_Q]/mL Solution/ Drops, 30 mL — NDC 63479-0703-01 package photo

G03 TEST-MET ADENOSINE TRIPHOSPHATE, AMMONIUM CHLORIDE, APIS MELLIFERA, BAPTISIA TINCTORIA ROOT, CALCIUM FLUORIDE, CAMPHOR (NATURAL), CITRULLUS COLOCYNTHIS FRUIT PULP, SEQUOIA SEMPERVIRENS BARK, SPONGIA OFFICINALIS SKELETON, ROASTED, TESTOSTERONE 7 [hp_C]/mL; 1 [hp_Q]/mL; 2 [hp_Q]/mL; 12 [hp_X]/mL; 1 [hp_X]/mL; 7 [hp_C]/mL; 3 [hp_Q]/mL Solution/ Drops, 30 mL

by Apex Energetics Inc. · 30 mL in 1 BOTTLE, GLASS (63479-0703-1)
NDC 63479-0703-01
🏷️ FDA NDC (as labeled) 63479-0703-1 billing pads the package segment with a zero
OTC On market CIII
🗂️ 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) 63479-0703-1
Product NDC 63479-0703
11-digit billing NDC 63479070301
UNII 7S82P3R43Z, O3B55K4YKI, N20HL7Q941, 23H32AOH17, V812D4QF7Z, 1PIP394IID +4 more
UPC 0818960013073
SPL Set ID bcbabd20-1941-3f11-e053-2a95a90a06dc
Established class (EPC) Standardized Insect Venom Allergenic Extract; Androgen
Mechanism of action Androgen Receptor Agonists
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Bee Venoms; Androstanes
DEA schedule CIII
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1996-05-15
Route SUBLINGUAL
Dosage form SOLUTION/ DROPS
Substance APIS MELLIFERA; CALCIUM FLUORIDE; CAMPHOR (NATURAL); CITRULLUS COLOCYNTHIS FRUIT PULP; SEQUOIA SEMPERVIRENS BARK; SPONGIA OFFICINALIS SKELETON, ROASTED; TESTOSTERONE; BAPTISIA TINCTORIA ROOT; ADENOSINE TRIPHOSPHATE; AMMONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 63479-0703-1 — 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 → 63479-0703-01. 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 marketedMay 1996
DEA scheduleCIII
Product typeHuman Otc Drug
Portfolio110 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 product taken as drops under the tongue. It contains multiple plant and mineral substances along with testosterone, which are used in homeopathic practice based on traditional beliefs rather than clinical evidence evaluated by the FDA. Homeopathic products are regulated differently than standard drugs and are not proven effective by modern scientific standards. The individual ingredients in homeopathic formulations are prepared through serial dilution according to homeopathic methods.

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
G03 Test-Met 7 [hp_C]/mL; 1 [hp_Q]/mL; 2 [hp_Q]/mL; 12 [hp_X]/mL; 1 [hp_X]/mL; 7 [hp_C]/mL; 3 [hp_Q]/mLthis 63479-0703-01 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

🏛️
1996
On the market since
May 1996
📍
2026
Currently FDA-listed
30 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 NDCDescription Marketing startStatus
63479-0703-01 You're viewing this 30 mL in 1 BOTTLE, GLASS (63479-0703-1) 1996-05-15 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

G03 TEST-MET ADENOSINE TRIPHOSPHATE, AMMONIUM CHLORIDE, APIS MELLIFERA, BAPTISIA TINCTORIA ROOT, CALCIUM FLUORIDE, CAMPHOR (NATURAL), CITRULLUS COLOCYNTHIS FRUIT PULP, SEQUOIA SEMPERVIRENS BARK, SPONGIA OFFICINALIS SKELETON, ROASTED, TESTOSTERONE 7 [hp_C]/mL; 1 [hp_Q]/mL; 2 [hp_Q]/mL; 12 [hp_X]/mL; 1 [hp_X]/mL; 7 [hp_C]/mL; 3 [hp_Q]/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) — 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 63479-0703-1, 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: 63479-0703-01, written without dashes as 63479070301. 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 63479-0703-01, the first segment (63479) is the labeler code FDA assigned to Apex Energetics Inc.; the middle segment (0703) 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 31 words ▾

Uses: For temporary relief of minor: great weakness and debility* poor concentration* low libido* weakness of the limbs* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

⏱️ Dosage and Administration 38 words ▾

Directions: Adults & children ages 12 years and over: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

⚠️ Warnings 79 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 great weakness and debility, poor concentration, low libido, weakness of the limbs, or other symptoms do not improve within 7 days or are accompanied by fever.

🧪 Active Ingredient 111 words ▾

Active Ingredients Adenosine Triphosphate 5X Ammonium Muriaticum 1LM 4C 5C 6C Apis Mellifica 2X 3X 6X 8X 12X 1C 2C 3C 5C 6C 7C Baptisia Tinctoria 4C 5C 6C Calcarea Fluorica 1LM Camphora 2LM Colocynthis 3X 6X 8X 12X 2C 3C 5C 6C 7C Sequoia Gigantea Bark 1X Spongia Tosta 2X 3X 6X 8X 12X 1C 2C 3C 5C 6C 7C Testosterone 3LM Adenosine Triphosphate 5X Calcarea Phosphorica 1LM Cinchona Officinalis 2X 3X 6X 8X 12X 1C 2C 3C 5C 6C 7C Crocus Sativus 2LM Phosphorus 12X 15X 24X 30X 60X 7C 9C 12C 15C 18C 30C Viscum Album Fruiting Top 2X 3X 6X 8X 12X 2C 3C 5C 6C 7C

🧪 Inactive Ingredients 6 words ▾

alcohol (20% by volume), distilled water

🎯 Purpose 30 words ▾

For temporary relief of minor: great weakness and debility* poor concentration* low libido* weakness of the limbs* *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 ↗
← 63479-0627-01 · Apex 63479-0705-01 · Apex →
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.