Drugplain

Saponaria officinalis 6 [hp_X]/1

SAPONARIA OFFICINALIS ROOT · PELLET · Laboratoires Boiron

No Recall History
Plain English

Saponaria officinalis is a pellet containing saponaria officinalis root at 6 [hp_X]/1, taken oral. Manufactured by Laboratoires Boiron.

Key Facts

Brand Name
Saponaria officinalis
Generic Name
SAPONARIA OFFICINALIS ROOT
NDC Code (Product)
0220-4562
Manufacturer
Laboratoires Boiron
Strength
6 [hp_X]/1
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

Skin Rash With Itching*

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 Saponaria officinalis used for?

Saponaria officinalis contains SAPONARIA OFFICINALIS ROOT. It is a pellet taken oral. Consult your doctor for specific uses.

Is Saponaria officinalis a controlled substance?

Saponaria officinalis is not classified as a controlled substance by the DEA.

What is the generic name for Saponaria officinalis?

The generic name for Saponaria officinalis is SAPONARIA OFFICINALIS ROOT. There are 1 other brand versions of SAPONARIA OFFICINALIS ROOT.

What is the NDC code for Saponaria officinalis 6 [hp_X]/1?

The NDC (National Drug Code) for Saponaria officinalis 6 [hp_X]/1 is 0220-4562, listed by Laboratoires Boiron.

Product NDC

0220-4562

Package NDC

0220-4562-41

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

Data from openFDA · Public domain (CC0 1.0)