DailyMed label
Cell Well
DailyMed label · JoyWell Co LLC · version 1
Key facts
| Product | Cell Well |
|---|---|
| Labeler | JoyWell Co LLC |
| Document type | HUMAN OTC DRUG LABEL |
| Active ingredients | CALCIUM FLUORIDE, CALCIUM PHOSPHATE, UNSPECIFIED FORM, CALCIUM SULFATE, UNSPECIFIED FORM, FERROSOFERRIC PHOSPHATE, MAGNESIUM CARBONATE, MAGNESIUM PHOSPHATE ANHYDROUS, OYSTER SHELL CALCIUM CARBONATE, CRUDE, POTASSIUM CHLORIDE, POTASSIUM PHOSPHATE, UNSPECIFIED FORM, POTASSIUM SULFATE, SILICON DIOXIDE, SODIUM CHLORIDE and 2 more |
| Active ingredient UNIIs | 0E53J927NA, 0YPR65R21J, 1K573LC5TV, 2E32821G6I, 451W47IQ8X, 660YQ98I10, 70WT22SF4B, 91GQH8I5F7, 97Z1WI3NDX, B7862WZ632, ETJ7Z6XBU4, O3B55K4YKI and 2 more |
| Route | ORAL |
| NDC package codes | 85946-0001-1 |
| Effective date | Dec 11, 2025 |
| Set ID | 592c1f48-21c8-4ff5-8818-046662c9effe |
At a glance
- 1–9 NDC package codes
- 10–99 Active ingredients
- None Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: