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Cell Well Calcium Carbonica,Calcium Fluoratum,Calcium Phosphoricum,Calcium Sulphuricum,Ferrum Phosphoricum,Kalium Muriaticum,Kalium Phosphoricum,Kalium Sulphuricum,Magnesium Carbonica,Magnesium Phosphoricum,Natrum Muriaticum,Natrum Phosphoricum,Natrum Sulphuricum,S 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60m Liquid, 60 mL — NDC 85946-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Cell Well Calcium Carbonica,Calcium Fluoratum,Calcium Phosphoricum,Calcium Sulphuricum,Ferrum Phosphoricum,Kalium Muriaticum,Kalium Phosphoricum,Kalium Sulphuricum,Magnesium Carbonica,Magnesium Phosphoricum,Natrum Muriaticum,Natrum Phosphoricum,Natrum Sulphuricum,S 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60m Liquid, 60 mL — NDC 85946-0001-1 (Billing 85946-0001-01)

by JoyWell Co LLC · 60 mL in 1 BOTTLE, DROPPER

This is a package of 60 mL of Cell Well Calcium Carbonica,Calcium Fluoratum,Calcium Phosphoricum,Calcium Sulphuricum,Ferrum Phosphoricum,Kalium Muriaticum,Kalium Phosphoricum,Kalium Sulphuricum,Magnesium Carbonica,Magnesium Phosphoricum,Natrum Muriaticum,Natrum Phosphoricum,Natrum Sulphuricum,S 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60m Liquid from JoyWell Co LLC, marketed since Nov 2025 and currently FDA-listed. It is this product's only package size.

NDC 85946-0001-01
🏷️ FDA NDC (as labeled) 85946-0001-1 billing pads the package segment with a zero
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 85946-0001-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85946 labeler · 0001 product · 1 package
Package marketed since
Nov 19, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0850077245015
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85946-0001-1
Product NDC 85946-0001
11-digit billing NDC 85946000101
UNII 2E32821G6I, O3B55K4YKI, 97Z1WI3NDX, WAT0DDB505, 91GQH8I5F7, 660YQ98I10 +8 more
UPC 0850077245015
SPL Set ID 592c1f48-21c8-4ff5-8818-046662c9effe
Established class (EPC) Blood Coagulation Factor; Cations; Increased Large Intestinal
Physiologic effect Increased Coagulation Factor Activity
Chemical class Calcium; Divalent
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-11-19
Route ORAL
Dosage form LIQUID
Substance OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; CALCIUM PHOSPHATE, UNSPECIFIED FORM; CALCIUM SULFATE, UNSPECIFIED FORM; FERROSOFERRIC PHOSPHATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, UNSPECIFIED FORM; POTASSIUM SULFATE; MAGNESIUM CARBONATE; MA
Why two NDCs? The FDA registers this code as 85946-0001-1 — 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 → 85946-0001-01. 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?

Cell Well is a liquid homeopathic product taken by mouth that contains twelve mineral salts and compounds in homeopathic dilutions. These ingredients, which include calcium salts, potassium salts, magnesium salts, sodium salts, and iron phosphate, are used in homeopathic practice according to homeopathic tradition rather than established medical evidence. Homeopathic products are not evaluated by the FDA for effectiveness or safety. This product is marketed as an unapproved homeopathic preparation.

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
85946-0001-01 You're viewing this Main listing 60 mL in 1 BOTTLE, DROPPER 2025-11-19 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cell Well 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mthis 85946-0001-01 JoyWell 60 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

🏛️
2025
On the market since
Nov 2025
📍
2026
Currently FDA-listed
1 year 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 PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • 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.

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

The official label also statesOrganic Glycerin, Purified water

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

LabelerJoyWell Co LLC
Labeler code85946
First marketedNov 2025
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from JoyWell Co LLC labeler code 85946

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Uses Encourages healthy mineral levels and tissue repair during periods of stress, fatigue or recovery.

⏱️ Dosage and Administration 29 words ▾

Directions Adults take 1 dropper sublingually 2-4 times daily. Kids 12-17 years of age take ½ dropper 2-3 times daily. Kids under 12, please consult with your healthcare provider.

⚠️ Warnings 23 words ▾

Warnings For oral use only. If pregnant or breast-feeding, ask a health care professional before use. Keep out of the reach of children.

🧪 Active Ingredient 109 words ▾

Active ingredients Purpose Calcium Carbonica 6X 7.14% bone growth, teething* Calcium Fluoratum 6X 7.14% connective tissue* Calcium Phosphoricum 6X 7.14% skin healing, acne* Calcium Sulphuricum 6X 7.14% metabolism, resilience* Ferrum Phosphoricum 6X 7.14% inflammation, immunity* Kalium Muriaticum 6X 7.14% congestion, eruptions* Kalium Phosphoricum 6X 7.14% nerves, sleep* Kalium Sulphuricum 6X 7.14% skin, respiration* Magnesium Carbonica 6X 7.14% digestion, irritability* Magnesium Phosphoricum 6X 7.14% cramps, spasms* Natrum Muriaticum 6X 7.14% headaches, emotions* Natrum Phosphoricum 6X 7.14% digestion, joints* Natrum Sulphuricum 6X 7.14% liver, detox* Silicea 6X 7.14% skin health, immunity* * Claims based on homeopathic practice are not accepted medical evidence.

These claims have not been evaluated by the FDA.

🧪 Inactive Ingredients 6 words ▾

Inactive ingredients Organic Glycerin, Purified water

📄 Package Label / Principal Display Panel 6 words ▾

Product label image description image description

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

Cell Well Calcium Carbonica,Calcium Fluoratum,Calcium Phosphoricum,Calcium Sulphuricum,Ferrum Phosphoricum,Kalium Muriaticum,Kalium Phosphoricum,Kalium Sulphuricum,Magnesium Carbonica,Magnesium Phosphoricum,Natrum Muriaticum,Natrum Phosphoricum,Natrum Sulphuricum,S 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60mL; 6 [hp_X]/60m 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 JoyWell Co LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
JoyWell Co LLC 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.
← 85945-0001-01 · Through 85946-0002-01 · JoyWell →
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.