Home › NDC Lookup › Ingredients › Calc Carb, Chenopodium Anth, Cina, Croto... › 61626-0107-04
🧴image loading
(from DailyMed)

Para Solve Calc carb, Chenopodium anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc corros, Nat phos, Santoninum, Senna, Spigelia anth, Stannum met, Tanacetum, Teuricum mar, Zingiber 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL Liquid, 59 mL

by NET Remedies · 59 mL in 1 BOTTLE (61626-0107-4)
NDC 61626-0107-04
🏷️ FDA NDC (as labeled) 61626-0107-4 billing pads the package segment with a zero
Rx only On market Non-controlled
🗂️ Data synced Sep 24, 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) 61626-0107-4
Product NDC 61626-0107
11-digit billing NDC 61626010704
UNII 2E32821G6I, 4H5RSU087I, 28M1820ACT, 0HK2GZK66E, C0ZK0RRF5X, 7556HJ7587 +11 more
SPL Set ID a58f6134-67f0-4691-8e9e-a93f48669d6a
Established class (EPC) Non-Standardized Plant Allergenic Extract; Non-Standardized Food Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Plant Proteins; Food Additives
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-12-04
Route ORAL
Dosage form LIQUID
Substance OYSTER SHELL CALCIUM CARBONATE, CRUDE; DYSPHANIA AMBROSIOIDES; ARTEMISIA CINA PRE-FLOWERING TOP; CROTON TIGLIUM SEED; DRYOPTERIS FILIX-MAS ROOT; GAMBOGE; PUNICA GRANATUM ROOT BARK; LYCOPODIUM CLAVATUM SPORE; MERCURIC CHLORIDE; SODIUM PHOSPHATE, DIBASIC, H
Why two NDCs? The FDA registers this code as 61626-0107-4 — 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 → 61626-0107-04. 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

LabelerNET Remedies
Labeler code61626
First marketedDec 2018
Product typeHuman Prescription Drug
Portfolio15 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?

Para Solve is an unapproved homeopathic liquid taken by mouth that contains multiple plant and mineral ingredients. In homeopathic practice, these ingredients are traditionally prepared and combined to address parasitic concerns, digestive upset, and related conditions. Homeopathic products are marketed based on traditional use rather than clinical evidence evaluated by the FDA. This product is not proven effective by modern medical standards.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesINACTIVE INGREDIENTS : Citric acid, Potassium sorbate, Purified water. Free of Alcohol, Sugar, Sodium, Yeast and Gluten.

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.

💲 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
Para Solve 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mLthis 61626-0107-04 NET 59 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

🏛️
2018
On the market since
Dec 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
61626-0107-04 You're viewing this 59 mL in 1 BOTTLE (61626-0107-4) 2018-12-04 Active

🧭 About this NDC listing & data coverage

Finished prescription product Homeopathic listing

About homeopathic listings

Para Solve Calc carb, Chenopodium anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc corros, Nat phos, Santoninum, Senna, Spigelia anth, Stannum met, Tanacetum, Teuricum mar, Zingiber 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL; 12 [hp_X]/59.1mL 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) ✓ 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 61626-0107-4, 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: 61626-0107-04, written without dashes as 61626010704. 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 61626-0107-04, the first segment (61626) is the labeler code FDA assigned to NET Remedies; the middle segment (0107) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) 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 NET Remedies. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
NET Remedies 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 a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
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.

📄 Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, 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 57 words ▾

​INDICATIONS FOR USE ​: For the temporary relief of gastrointestinal symptoms such as gas, bloating, stomach upset, abdominal discomfort which may be accompanied by pale face or circles under the eyes, bad breath, bariable appetite, localized ithching, postnasal drip, canker sores. irritability, back pain, resltess sleep, and sensitivity in lower right abdominal area. Temporary relief of cough.**

⏱️ Dosage and Administration 34 words ▾

DIRECTIONS: Spray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as directed by a licensed health care practicioner. When appropriate, also spray externally on complaint area 3 times daily.

⚠️ Warnings 52 words ▾

WARNINGS: • If symptoms persist or worsen , seek advice of licensed health care practicioner. • If pregnant or nursing , take on only advice of licensed health care practicioner. • Keep this and all medication out of reach of children. • Keep this and all medication out of reach of children.

🧪 Active Ingredient 76 words ▾

​ACTIVE INGREDIENTS (HPUS*) ​: Contains equal volumes of each in 12X, 30X, and 100X potencies: Calc carb, Chenopodium anth, Cina, Croton, Filix Mas, Gambogia, Granatum, Lycopodium, Merc corros, Nat phos, Santoninum, Senna, Spigelia anth, Stannum met, Tanacetum, Teucrium mar, Zingiber. (*) The letters "HPUS" indicate that the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States. (**) Claims based on traditional homeopathic practice.

Not accepted medical evidence. Not FDA evaluated.

🧪 Inactive Ingredients 17 words ▾

INACTIVE INGREDIENTS : Citric acid, Potassium sorbate, Purified water. Free of Alcohol, Sugar, Sodium, Yeast and Gluten.

🎯 Purpose 56 words ▾

INDICATIONS FOR USE: For the temporary relief of gastrointestinal symptoms such as gas, bloating, stomach upset, abdominal discomfort which may be accompanied by pale face or circles under the eyes, bad breath, bariable appetite, localized ithching, postnasal drip, canker sores. irritability, back pain, resltess sleep, and sensitivity in lower right abdominal area. Temporary relief of cough.**

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 61626-0106-04 · NET 61626-0108-04 · NET →
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.