Drugplain

Lapis albus 6 [hp_C]/6[hp_C]

CALCIUM HEXAFLUOROSILICATE · PELLET · Boiron

No Recall HistoryCurrently in Shortage
Plain English

Lapis albus is a pellet containing calcium hexafluorosilicate at 6 [hp_C]/6[hp_C], taken oral. Manufactured by Boiron.

Key Facts

Brand Name
Lapis albus
Generic Name
CALCIUM HEXAFLUOROSILICATE
NDC Code (Product)
0220-3053
Manufacturer
Boiron
Strength
6 [hp_C]/6[hp_C]
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
03/03/1983

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Rx Only*

Dosage & Administration

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Frequently Asked Questions

What is Lapis albus used for?

Lapis albus contains CALCIUM HEXAFLUOROSILICATE. It is a pellet taken oral. Consult your doctor for specific uses.

Is Lapis albus a controlled substance?

Lapis albus is not classified as a controlled substance by the DEA.

What is the generic name for Lapis albus?

The generic name for Lapis albus is CALCIUM HEXAFLUOROSILICATE. There are no other listed brand versions of CALCIUM HEXAFLUOROSILICATE.

What is the NDC code for Lapis albus 6 [hp_C]/6[hp_C]?

The NDC (National Drug Code) for Lapis albus 6 [hp_C]/6[hp_C] is 0220-3053, listed by Boiron.

Product NDC

0220-3053

Package NDC

0220-3053-41

Other Lapis albus Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)