Home › NDC Lookup › Ingredients › Meb Puri-Vega › 81488-0013-10
MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/ Liquid, 1000 mL — NDC 81488-0013-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/ Liquid, 1000 mL — NDC 81488-013-10 (Billing 81488-0013-10)

by Kadesh Incoporation Co,Ltd · 1000 mL in 1 BOTTLE

This is a package of 1,000 mL of MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/ Liquid from Kadesh Incoporation Co,Ltd, marketed since Aug 2023 and currently FDA-listed.

NDC 81488-0013-10
🏷️ FDA NDC (as labeled) 81488-013-10 billing pads the product segment with a zero
This package
Contains1000 mL Pack sizes2 compare ↓
Product page 81488-0013-03 Also comes in: 300 ml 81488-013-03
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 81488-013-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
81488 labeler · 013 product · 10 package
Package marketed since
Aug 22, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8148801310 3
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 81488-013-10
Product NDC 81488-013
11-digit billing NDC 81488001310
UNII O3B55K4YKI, SK47B8698T, 8M4L3H2ZVZ, J41CSQ7QDS, 91GQH8I5F7, 02F3473H9O +2 more
SPL Set ID 03865989-3034-10fc-e063-6394a90ac80b
Established class (EPC) Calculi Dissolution Agent; Osmotic Activity
Mechanism of action Magnesium Ion Exchange Activity
Physiologic effect Increased Large Intestinal Motility; Inhibition Large Intestine Fluid/Electrolyte Absorption; Inhibition Small Intestine Fluid/Electrolyte Absorption
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-08-22
Route ORAL
Dosage form LIQUID
Substance CALCIUM FLUORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; SODIUM NITRATE; ZINC; FERROSOFERRIC PHOSPHATE; MAGNESIUM CHLORIDE; SILICON DIOXIDE; SULFUR
Why two NDCs? The FDA registers this code as 81488-013-10 — a 5-3-2 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 product segment → 81488-0013-10. 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.

Clinical

🧪 What is this product?

MEB Puri-vega is an oral liquid homeopathic product containing multiple mineral and elemental ingredients including calcium fluoride, magnesium salts, zinc, sulfur, and sodium nitrate. In homeopathic practice, these substances are traditionally used in highly diluted form for various wellness purposes, though homeopathic products are not evaluated by the FDA for effectiveness. This product is marketed based on homeopathic tradition rather than clinical evidence of efficacy.

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.

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.
Try another pack size: 300 ml
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
81488-0013-03 81488-013-03 Main listing 300 mL in 1 BOTTLE 2023-08-22 — Active
81488-0013-10 You're viewing this 1000 mL in 1 BOTTLE 2023-08-22 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 1000 mL — 1000 ml in 1 bottle.
How does this package differ from NDC 81488-0013-03?
Both are MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/ Liquid — the drug itself is identical. This page's package is the 1000 mL one, while NDC 81488-0013-03 is the 300 ml package.
What NDC number is used to bill for this package of MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/ Liquid?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/this 81488-0013-10 Kadesh 1000 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

🏛️
2023
On the market since
Aug 2023
📍
2026
Currently FDA-listed
3 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.

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 LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII S4255P4G5M
    Calcium silicate is a white powder made from calcium and silicon compounds. It acts as an anti-caking agent and flow aid, helping powder ingredients move smoothly during tablet or capsule manufacturing.
  • UNII 0UV74P3R0J
    A cerium-based chemical compound used as a colorant and opacifying agent in medications. It provides a white to off-white color and helps control light transmission in capsules and tablets.
  • UNII 0I2XIN602U
    Ferric chloride hexahydrate is an iron compound used in medicine as a coagulant and hemostatic agent. It helps control bleeding by causing blood to clot, typically in topical formulations or solutions applied directly to wound sites.
  • UNII E1UOL152H7
    Iron is a metallic element used as a colorant in medications. It produces red, yellow, brown, or black shades in tablets and capsules depending on the iron compound form.
  • UNII 24H4NWX5CO
    Kaolin is a naturally occurring clay mineral. It's used in tablets and capsules as a filler and absorbent to add bulk, improve texture, and help bind ingredients together.
  • UNII 42Z2K6ZL8P
    Manganese is a metallic mineral element. It's used in some formulations as a colorant or trace component in mineral supplement products.
  • UNII 27YLU75U4W
    A mineral element used in small amounts as a buffering agent to help stabilize the pH balance of a medication, keeping it from becoming too acidic or basic.
  • UNII J86L1GUL6K
    Potassium silicate is a mineral compound used as a binder and anti-caking agent. It helps hold tablet ingredients together and prevents clumping or moisture absorption during storage.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII D1JT611TNE
    A metallic element used as a white colorant and opacifying agent in tablets and capsules. It provides color consistency and helps make medicines visually uniform.
  • UNII 00J9J9XKDE
    Vanadium is a mineral element used in small amounts as a stabilizer or processing agent in some pharmaceutical formulations to help maintain product consistency and shelf life.

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

The official label also statesAlumina Silicata, Calcarea Silicata, Natrum Muriaticum, Alumina, Ferrum Metallicum, Ferrum Muriaticum, Kali Silicatum, Titanium Metallicum, Phosphorus, Cerium Oxalicum, Maganum Metallicum, Vanadium Metallicum

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.

Manufacturer & labeler

LabelerKadesh Incoporation Co,Ltd
Labeler code81488
First marketedAug 2023
Product typeHuman Otc Drug
Portfolio12 products on file

More NDCs from Kadesh Incoporation Co,Ltd labeler code 81488

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.

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 📄 Ask a Doctor Before Use If 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 100 words ▾

MEB Puri-Vega is potent mineral concentrate with exceptional health benefits. Offers unparalleled support for overall well-being, including asthma, immune deficiency, rhinitis, diabetes and more.” Usage: Puri-Vega is a potent mineral concentrate enriched with various health benefits. Extracted from beneficial minerals known for their exceptional absorbability in the human body, this health blend offers unparalleled support for overall well-being.

The natural healing and preventive properties of Puriton Mineral, a 100% pure mineral extract sourced from nature provides excellent effects in conditions related to Inflammation-Related Issues that can lead to many other sickness, Internal Diseases, and Ulcers that can lead to tumors.

⏱️ Dosage and Administration 118 words ▾

Direction Take 30ml once daily in the morning on an empty stomach. For effective absorption, do not swallow immediately; hold under the tongue for 2-3 minutes before swallowing. It can also be consumed by mixing 1:1 with water, as needed.

Usage as an Additive for Herbal Medicine: Mix 30 ml or 50 ml with medication as an additive when boiling. Removes toxins from the medication. Aids in nanonization, enabling better absorption of medicinal ingredients.

Provides concentrated extraction without the need for re-boiling. Preserves the minerals without any loss or change in properties. For oral inflammation: Gargle with Puri-Vega 10 ml for 10 minutes or more, three times a day, to help with oral inflammation caused by weakened immunity.

⚠️ Warnings 37 words ▾

Individuals with specific sensitivities to ingredients or allergies should check the list of ingredients before consumption. If your symptoms do not improve and worsen even after 7 days, discontinue use and consult a doctor for further advice.

🧪 Active Ingredient 13 words ▾

Sulphur, Ferrum Phosphoricum, Natrum Nitricum, Calcarea Fluorata, Magnesia Sulphurica, Magnesia Muriatica, Zincum Metalicum

🧪 Inactive Ingredients 22 words ▾

Alumina Silicata, Calcarea Silicata, Natrum Muriaticum, Alumina, Ferrum Metallicum, Ferrum Muriaticum, Kali Silicatum, Titanium Metallicum, Phosphorus, Cerium Oxalicum, Maganum Metallicum, Vanadium Metallicum

🎯 Purpose 47 words ▾

Active Ingredients Purpose Silicea 4X HPUS ………………………………….. Ulcers Sulphur 4X HPUS………………………………….. Tumour Ferrum Phosphoricum 7X HPUS.………………… Inflammation, Ulcers Natrum Nitricum 5X HPUS……………………….. Inflammation Calcarea Fluorata 6X HPUS……………………… Inflammation, Tumor Magnesia Sulphurica 7X HPUS …………………. Internal Disease Magnesia Muriatica 7X HPUS…………………. Inflammation Zincum Metalicum 8X …………………………….. Internal Disease

📄 Ask a Doctor Before Use If 17 words ▾

If pregnant, breastfeeding, or undergoing treatment for any medical condition, please consult a physician before taking it.

📄 Recent Major Changes 6 words ▾

Typo fixed in Indication and Usage

📄 Package Label / Principal Display Panel 8 words ▾

MEB Vega-Puri. NDC: 81488-013-03 MEB Vega-Puri. NDC: 81488-013-03

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

MEB Puri-vega 6 [hp_X]/300mL; 7 [hp_X]/300mL; 5 [hp_X]/300mL; 8 [hp_X]/300mL; 7 [hp_X]/300mL; 7 [hp_X]/300mL; 4 [hp_X]/300mL; 4 [hp_X]/ 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) ✓ 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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Kadesh Incoporation Co,Ltd. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 300 ml (81488-0013-03). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Kadesh Incoporation Co,Ltd 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.
← 81488-0012-03 · Kadesh 81493-0201-80 · Priia →
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.