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Benefit Plus Drops Kidney (Suis), Abrotanum, Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Glandula Suprarenalis Suis, Graphites, Helleborus Niger, Hepar Suis, Hypothalamus Suis, Ignatia Amara, Lycopodium Clavatum, Secale Cornutum, Silice 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL Liquid, 30 mL — NDC 72349-0001-1 (Billing 72349-0001-01)

by Gulf Coast Wellness Center · 30 mL in 1 BOTTLE, DROPPER

This is a package of 30 mL of Benefit Plus Drops Kidney (Suis), Abrotanum, Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Glandula Suprarenalis Suis, Graphites, Helleborus Niger, Hepar Suis, Hypothalamus Suis, Ignatia Amara, Lycopodium Clavatum, Secale Cornutum, Silice 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL Liquid from Gulf Coast Wellness Center, no longer marketed (first marketed Aug 2018), no longer in the FDA NDC Directory, this package's marketing ended Sep 2026. It is this product's only package size.

NDC 72349-0001-01
🏷️ FDA NDC (as labeled) 72349-0001-1 billing pads the package segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 10, 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 72349-0001-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72349 labeler · 0001 product · 1 package
Package marketed since
Aug 17, 2018
Package marketing ended
Sep 11, 2026
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 7234900011 0
FDA record last changed
Sep 10, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Sep 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72349-0001-1
Product NDC 72349-0001
11-digit billing NDC 72349000101
UNII X7BCI5P86H, QG07G580U0, Y0F0BU8RDU, EL5GJ3U77E, 2E32821G6I, 91D9GV0Z28 +11 more
SPL Set ID a12444e6-d58d-40d5-b5ed-e9725f1c064b
Established class (EPC) Blood Coagulation Factor; Cations; Phosphate Binder
Mechanism of action Phosphate Chelating Activity
Physiologic effect Increased Coagulation Factor Activity
Chemical class Calcium; Divalent
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Sep 2026)
Marketing start 2018-08-17
Marketing end 2026-09-11
Route ORAL
Dosage form LIQUID
Substance PORK KIDNEY; ARTEMISIA ABROTANUM FLOWERING TOP; SEMECARPUS ANACARDIUM JUICE; BARIUM CHLORIDE DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; SUS SCROFA ADRENAL GLAND; GRAPHITE; HELLEBORUS NIGER ROOT; PORK LIVER; SUS SCROFA HY
Why two NDCs? The FDA registers this code as 72349-0001-1 — 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 → 72349-0001-01. 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.

Clinical

🧪 What is this product?

Benefit Plus Drops Kidney is an unapproved homeopathic liquid taken by mouth. It contains a mixture of plant extracts, minerals, and animal-derived substances that are traditionally used in homeopathic practice for support related to kidney function and overall wellness. Homeopathic products are marketed based on homeopathic tradition rather than clinical evidence, and the FDA does not evaluate them for effectiveness or safety the way it does conventional medicines.

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.
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
72349-0001-01 You're viewing this Main listing 30 mL in 1 BOTTLE, DROPPER 2018-08-17 Sep 11, 2026 Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Benefit Plus Drops 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mLthis 72349-0001-01 Gulf 30 ml — — Discontinued —
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

🏛️
2018
On the market since
Aug 2018
📍
2026
Currently FDA-listed
8 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.

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.

Manufacturer & labeler

LabelerGulf Coast Wellness Center
Labeler code72349
First marketedAug 2018
Product typeHuman Otc Drug
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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

INDICATIONS: Temporarily boosts metabolism, decreases appetite and promotes lean muscle mass.

⏱️ Dosage and Administration 27 words ▾

DIRECTIONS: 10 drops under the tongue, twice daily. Take 30 minutes before breakfast and dinner. Consult a physician for use in children under 12 years of age.

⚠️ Warnings 47 words ▾

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

🧪 Active Ingredient 84 words ▾

ACTIVE INGREDIENTS: Kidney (Suis) 8X, 12X, Abrotanum 8X, 12X, 30C, Anacardium Orientale 8X, 12X, 30C, Baryta Muriatica 8X, 12X, 30C, Calcarea Carbonica 8X, 12X, 30C, Calcarea Phosphorica 8X, 12X, 30C, Glandula Suprarenalis Suis 8X, 12X, 30C, Graphites 8X, 12X, 30C, Helleborus Niger 8X, 12X, 30C, Hepar Suis 8X, 12X, 30C, Hypothalamus Suis 8X, 12X, 30C, Ignatia Amara 8X, 12X, 30C, Lycopodium Clavatum 8X, 12X, 30C, Secale Cornutum 8X, 12X, 30C, Silicea 8X, 12X, 30C, Thymus (Suis) 8X, 12X, 30C, Thyroidinum (Suis) 8X, 12X, 30C.

🧪 Inactive Ingredients 6 words ▾

INACTIVE INGREDIENTS: Demineralized Water, 25% Ethanol

🎯 Purpose 11 words ▾

INDICATIONS: Temporarily boosts metabolism, decreases appetite and promotes lean muscle mass.

📄 Keep Out of Reach of Children 25 words ▾

KEEP OUT OF REACH OF CHILDREN: Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

📄 Questions or Comments 15 words ▾

QUESTIONS: Dist. By: Gulf Coast Wellness Center 2318 Pass Rd., Ste. 7C Biloxi, MS 39531

📄 Package Label / Principal Display Panel 17 words ▾

PACKAGE LABEL DISPLAY: NDC: 72349-0001-1 BENEFIT PLUS DROPS HOMEOPATHIC 1 FL OZ (30 ml) Benefit Plus Drops

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 No longer marketed (per FDA listing data)

About homeopathic listings

Benefit Plus Drops Kidney (Suis), Abrotanum, Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Glandula Suprarenalis Suis, Graphites, Helleborus Niger, Hepar Suis, Hypothalamus Suis, Ignatia Amara, Lycopodium Clavatum, Secale Cornutum, Silice 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 8 [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 — 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
Gulf Coast Wellness Center 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.
← 72347-0010-05 · Bruder 72358-0101-03 · Amphp, →
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.