NDC codes

FDA NDC Directory
Product NDC (as listed)85946-0001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85946-0001Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
85946-0001-1859460001018594600010160 mL in 1 BOTTLE, DROPPER (85946-0001-1)Marketed from Nov 19, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Cell Well
Generic name (nonproprietary)
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,silicea
Active ingredients
Oyster shell calcium carbonate, Crude — 6 [hp_X]/60mLCalcium fluoride — 6 [hp_X]/60mLCalcium phosphate, Unspecified form — 6 [hp_X]/60mLCalcium sulfate, Unspecified form — 6 [hp_X]/60mLFerrosoferric phosphate — 6 [hp_X]/60mLPotassium chloride — 6 [hp_X]/60mLPotassium phosphate, Unspecified form — 6 [hp_X]/60mLPotassium sulfate — 6 [hp_X]/60mLMagnesium carbonate — 6 [hp_X]/60mLMagnesium phosphate anhydrous — 6 [hp_X]/60mLSodium chloride — 6 [hp_X]/60mLSodium phosphate, Dibasic, Heptahydrate — 6 [hp_Q]/60mLSodium sulfate — 6 [hp_X]/60mLSilicon dioxide — 6 [hp_Q]/60mL
Dosage form
Liquid
Route
Oral
Labeler
JoyWell Co LLCNDC labeler code 85946
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Calcium (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)Potassium Compounds (Chemical structure)
Identifiers
Product ID 85946-0001_45ac3bd8-7e9b-d951-e063-6394a90aa039SPL ID 45ac3bd8-7e9b-d951-e063-6394a90aa039SPL set ID 592c1f48-21c8-4ff5-8818-046662c9effeUNII 2E32821G6I, O3B55K4YKI, 97Z1WI3NDX, WAT0DDB505, 91GQH8I5F7, 660YQ98I10, B7862WZ632, 1K573LC5TV, 0E53J927NA, XMK14ETW2D, 451W47IQ8X, 70WT22SF4B, 0YPR65R21J, ETJ7Z6XBU4UPC 0850077245015
Pharmacologic class
Blood Coagulation Factor; Osmotic Laxative; Phosphate Binder; Potassium Salt

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485946000101 followed by a unit qualifier and the quantity

Package 85946-0001-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85946-0001

What is NDC 85946-0001?
85946-0001 is the product NDC for Cell Well, Oyster shell calcium carbonate, Crude 6 [hp_X]/60mL + 13 more ingredients liquid, listed with the FDA by JoyWell Co LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
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,Silicea).
What is the active ingredient?
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, Magnesium phosphate anhydrous, Sodium chloride, Sodium phosphate, Dibasic, Heptahydrate, Sodium sulfate, Silicon dioxide.
Who is the labeler?
JoyWell Co LLC, NDC labeler code 85946. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cell Well?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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