Calcarea silicata (calcium silicate) NDC 0220-1095

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-1095Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-1095Add 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 NDC	11-digit (billing)	Package	Copy
0220-1095-41	00220109541	30 [hp_C] in 1 TUBE (0220-1095-41)Marketed from Mar 3, 1983

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Calcarea silicata
Generic name (nonproprietary): calcium silicate
Active ingredients: Calcium silicate — 30 [hp_C]/30[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 0220-1095_09be8cc8-b80d-4600-e063-6294a90a74a2SPL ID 09be8cc8-b80d-4600-e063-6294a90a74a2SPL set ID 849c4b62-8428-29b7-e053-2a91aa0aede3UNII S4255P4G5M
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

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

N400220109541 followed by a unit qualifier and the quantity

Package 00220-1095-41. 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 Nov 9, 2023.

Indications (excerpt from the label)

Weakness, fatigue with hypersensitivity to cold*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)