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Bio Chem Detox Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Triticum Aestivum, Xanthoxylum Fraxineum, Phytolacca Decandra, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (Suis), Thyroidinum 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL Spray, 30 mL

by BioActive Nutritional, Inc. · 30 mL in 1 PACKAGE (43857-0613-1)
NDC 43857-0613-01
🏷️ FDA NDC (as labeled) 43857-0613-1 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) 43857-0613-1
Product NDC 43857-0613
11-digit billing NDC 43857061301
UNII 1TH8Q20J0U, 2788Z9758H, 597E9BI3Z3, 4VBP01X99F, QBR70R4FBK, 4JS0838828 +12 more
SPL Set ID 3f9bd6c8-6fc9-4af1-8263-ab42f99fba37
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Dietary Proteins; Plant Proteins; Seed Storage Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-09-02
Route ORAL
Dosage form SPRAY
Substance BERBERIS VULGARIS ROOT BARK; GLYCYRRHIZA GLABRA; ARCTIUM LAPPA ROOT; FRANGULA PURSHIANA BARK; STILLINGIA SYLVATICA ROOT; TRIFOLIUM PRATENSE FLOWER; TRITICUM AESTIVUM WHOLE; ZANTHOXYLUM AMERICANUM BARK; PHYTOLACCA AMERICANA ROOT; SUS SCROFA ADRENAL GLAND;
Why two NDCs? The FDA registers this code as 43857-0613-1 — 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 → 43857-0613-01. 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

LabelerBioActive Nutritional, Inc.
Labeler code43857
First marketedSep 2021
Product typeHuman Otc Drug
Portfolio315 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 oral spray containing multiple plant extracts, minerals, and animal-derived substances. The product is marketed according to homeopathic tradition and has not been evaluated by the FDA for safety or effectiveness. In homeopathic practice, the ingredients are typically used to support general detoxification and lymphatic function, though homeopathic products are not recognized by conventional medicine as having proven clinical effects at their diluted potencies. This product is sold as an over-the-counter homeopathic remedy.

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
Bio Chem Detox 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mLthis 43857-0613-01 BioActive 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

🏛️
2021
On the market since
Sep 2021
📍
2026
Currently FDA-listed
5 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
43857-0613-01 You're viewing this 30 mL in 1 PACKAGE (43857-0613-1) 2021-09-02 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Bio Chem Detox Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Triticum Aestivum, Xanthoxylum Fraxineum, Phytolacca Decandra, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (Suis), Thyroidinum 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL; 3 [hp_X]/mL SPRAY 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 — Not published for this NDC No photo available yet for this listing.
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 43857-0613-1, 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: 43857-0613-01, written without dashes as 43857061301. 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 43857-0613-01, the first segment (43857) is the labeler code FDA assigned to BioActive Nutritional, Inc.; the middle segment (0613) 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 BioActive Nutritional, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
BioActive Nutritional, 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 28 words ▾

USES: For the temporary relief of numbness, tingling, trembling, paralysis, short of breath, burning eyes.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

⏱️ Dosage and Administration 17 words ▾

DIRECTIONS: • 1 spray orally, 3 times a day or as directed by a health care professional.

⚠️ Warnings 50 words ▾

WARNINGS: If pregnant or breast-feeding, ask a health care 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 124 words ▾

ACTIVE INGREDIENTS: Aconitum Napellus 12X, 30X, 200X, 30C, Agaricus Muscarius 30C, Arsenicum Album 12X, 30X, 200X, 30C, Belladonna 12X, 30X, 200X, 30C, Berberis Vulgaris 3X, Carbo Vegetabilis 12X, 30X, 200X, 30C, Cinchona Officinalis 12X, 30X, 200X, 30C, Conium Maculatum 12X, 30X, 200X, 30C, Curare 30C, 200C, Glandula Suprarenalis Suis 6X, Glycyrrhiza Glabra 3X, Hepar Suis 6X, Lachesis Mutus 30C, Lappa Major 3X, Lycopodium Clavatum 12X, Lymph Node Suis 6X, Mercurius Corrosivus 12X, 30X, 200X, 30C, Nitricum Acidum 12X, 30C, Nux Vomica 12X, Phosphorus 12X, 30X, 200X, 30C, Phosphoricum Acidum 12X, Physostigma Venenosum 30C, Phytolacca Decandra 4X, Rhamnus Purshiana 3X, Stillingia Sylvatica 3X, Sulphur 12X, 30X, 200X, 30C, Tabacum 12X, 30X, 200X, 30C, Thyroidinum Suis 6X, Trifolium Pratense 3X, Triticum Aestivum 3X, Xanthoxylum Fraxineum 3X.

🧪 Inactive Ingredients 11 words ▾

INACTIVE INGREDIENTS: Citric Acid, Demineralized Water, Ethanol 5%, Glycerin, Sodium Benzoate.

🎯 Purpose 147 words ▾

PURPOSE: Aconitum Napellus - numbness,** Agaricus Muscarius - itching,** Arsenicum Album – burning pain,** Belladonna – throbbing pain,** Berberis Vulgaris - analgesic,** Carbo Vegetabilis – respiratory problems,** Cinchona Officinalis – weak muscle,** Conium Maculatum - weakness,** Curare – burning eyes,** Glandula Suprarenalis Suis – lung support,** Glycyrrhiza Glabra - inflammation,** Hepar Suis – circulation support,** Lachesis Mutus - headache,** Lappa Major - numbness,** Lycopodium Clavatum – skin irritation,** Lymph Node Suis - fatigue,** Mercurius Corrosivus - inflammation,** Nitricum Acidum – sharp pain,** Nux Vomica - numbness,** Phosphorus - weakness,** Phosphoricum Acidum - headache,** Physostigma Venenosum - spasms,** Phytolacca Decandra - conjunctivitis,** Rhamnus Purshiana - detoxification,** Stillingia Sylvatica - tremors,** Sulphur – heavy menses,** Tabacum – circulatory issues,** Thyroidinum Suis - fatigue,** Trifolium Pratense - headache,** Triticum Aestivum – anti-inflammatory,** Xanthoxylum Fraxineum – dry cough** **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 ↗
← 43857-0612-01 · BioActive 43857-0614-01 · BioActive →
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.