![COLOCYNTHIS 3 [hp_X]/1 Pellet, 1,000-count — NDC 15631-0152-07 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=5ec7c1d2-7d5f-4cbe-ac5a-c4d8242a7a5b&name=Rxhomeo+-+Secondary-Packing+-+Blister+Pack.jpg)
COLOCYNTHIS 3 [hp_X]/1 Pellet, 1,000-count
by Rxhomeo Private Limited d.b.a. Rxhomeo, Inc · 1000 PELLET in 1 PACKAGE (15631-0152-7)
NDC 15631-0152-07
🏷️ FDA NDC (as labeled)
15631-0152-7
billing pads the package segment with a zero
This package
Contains1,000-count
Pack sizes8 compare ↓
Also comes in:
100 pellets 15631-0152-00
200 pellets 15631-0152-01
400 pellets 15631-0152-02
500 pellets 15631-0152-06
750 pellets 15631-0152-03
2500 pellets 15631-0152-04
12500 pellets 15631-0152-05
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
15631-0152-7
Product NDC
15631-0152
11-digit billing NDC
15631015207
UNII
23H32AOH17
UPC
8907460005526
SPL Set ID
5ec7c1d2-7d5f-4cbe-ac5a-c4d8242a7a5b
DEA schedule
Non-controlled
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2015-10-02
Route
ORAL
Dosage form
PELLET
Substance
CITRULLUS COLOCYNTHIS FRUIT PULP
Why two NDCs?
The FDA registers this code as 15631-0152-7 — 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 → 15631-0152-07. 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
LabelerRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Labeler code15631
First marketedOct 2015
Product typeHuman Otc Drug
Portfolio214 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 pellet taken by mouth containing colocynthis (the pulp from the colocynth fruit). In traditional homeopathic practice, colocynthis has been used to address digestive discomfort and cramping. Homeopathic products are marketed based on homeopathic tradition and principles rather than clinical evidence, and the FDA does not evaluate them for effectiveness or safety in the way it does other medicines.
Patient education
Supplement & herbal interactions
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.
💬 Questions about COLOCYNTHIS?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 system | Per each | 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.
Try another pack size:
100 pellets
200 pellets
400 pellets
500 pellets
750 pellets
2500 pellets
12500 pellets
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 |
|---|---|---|---|---|---|---|
| Colocynthis 3 [hp_X]this 15631-0152-07 | Rxhomeo | 1000 pellets | — | — | 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
🏛️
2015
On the market since
Oct 2015
📍
2026
Currently FDA-listed
11 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.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Colocynthis — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 28%
Female · 72%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 15631-0152-00 | 100 PELLET in 1 PACKAGE (15631-0152-0) | 2018-01-01 | Active |
| 15631-0152-01 | 200 PELLET in 1 PACKAGE (15631-0152-1) | 2018-01-01 | Active |
| 15631-0152-02 | 400 PELLET in 1 PACKAGE (15631-0152-2) | 2018-01-01 | Active |
| 15631-0152-03 | 750 PELLET in 1 PACKAGE (15631-0152-3) | 2018-01-01 | Active |
| 15631-0152-04 | 2500 PELLET in 1 PACKAGE (15631-0152-4) | 2018-01-01 | Active |
| 15631-0152-05 | 12500 PELLET in 1 PACKAGE (15631-0152-5) | 2018-01-01 | Active |
| 15631-0152-06 | 500 PELLET in 1 PACKAGE (15631-0152-6) | 2021-08-23 | Active |
| 15631-0152-07 You're viewing this | 1000 PELLET in 1 PACKAGE (15631-0152-7) | 2021-08-23 | Active |
You're viewing one of 8 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 15631-0152-07?
NDC 15631-0152-07 is a 1,000-count package — 1000 pellet in 1 package.
What is the difference between NDC 15631-0152-07 and NDC 15631-0152-00?
Both are COLOCYNTHIS 3 [hp_X]/1 Pellet — the drug itself is identical. NDC 15631-0152-07 is the 1,000-count package, while NDC 15631-0152-00 is the 100 pellets package.
What NDC number is used to bill for this package of COLOCYNTHIS 3 [hp_X]/1 Pellet?
Bill NDC 15631-0152-07 — the 11-digit billing format is 15631015207. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
Homeopathic listing
About homeopathic listings
COLOCYNTHIS 3 [hp_X]/1 PELLET 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 15631-0152-7, 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: 15631-0152-07, written without dashes as 15631015207. 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 15631-0152-07, the first segment (15631) is the labeler code FDA assigned to Rxhomeo Private Limited d.b.a. Rxhomeo, Inc; the middle segment (0152) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (07) 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 Rxhomeo Private Limited d.b.a. Rxhomeo, Inc. 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 7 other package presentations of this same product, including 100 pellets (15631-0152-00), 200 pellets (15631-0152-01), 400 pellets (15631-0152-02). 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?
Rxhomeo Private Limited d.b.a. Rxhomeo, 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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
INDICATIONS Condition listed above or as directed by the physician
⏱️ Dosage and Administration ▾
DOSAGE Adults- Take 4 or 6 Pellets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose.
⚠️ Warnings ▾
WARNINGS This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children Do not use if capseal is broken or missing. Close the cap tightly after use.
📦 Storage and Handling ▾
STORAGE Store in a cool dark place
🧪 Active Ingredient ▾
ACTIVE INGREDIENT COLOCYNTHIS HPUS 3X and higher
🧪 Inactive Ingredients ▾
INACTIVE INGREDIENTS Sucrose
🎯 Purpose ▾
USES USES: Temporary Relief - Spasm Pain* * Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.