NDC product
Cell Well
NDC 85946-0001 · JoyWell Co LLC
Key facts
| Product NDC | 85946-0001 |
|---|---|
| Proprietary name | Cell Well |
| Nonproprietary name | Calcium Carbonica, Calcium Fluoratum, Calcium Phosphoricum, Calcium Sulphuricum, Ferrum Phosphoricum, Kalium Muriaticum, Kalium Phosphoricum, Kalium Sulphuricum, Magnesium Carbonica, Magnesium Phosphoricum, Natrum Muriaticum, Natrum Phosphoricum and 2 more |
| Substances | 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 and 2 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | JoyWell Co LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE] and 7 more |
| Marketing start | Nov 19, 2025 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: