Drugplain

SCUTELLARIA LATERIFLORA 200 [kp_C]/200[kp_C]

SCUTELLARIA LATERIFLORA WHOLE · PELLET · Boiron

No Recall History
Plain English

SCUTELLARIA LATERIFLORA is a pellet containing scutellaria lateriflora whole at 200 [kp_C]/200[kp_C], taken oral. Manufactured by Boiron.

Key Facts

Brand Name
SCUTELLARIA LATERIFLORA
Generic Name
SCUTELLARIA LATERIFLORA WHOLE
NDC Code (Product)
0220-4600
Manufacturer
Boiron
Strength
200 [kp_C]/200[kp_C]
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
01/01/2025

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

alanine aminotransferase increased4 reports
blood calcium increased4 reports
blood magnesium increased4 reports
blood phosphorus increased4 reports
abnormal dreams1 reports
blood pressure increased1 reports
constipation1 reports
decreased appetite1 reports
diarrhoea1 reports
fatigue1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Relieves fatigue with frontal headaches * Uses: See symptoms on front panel.

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 SCUTELLARIA LATERIFLORA used for?

SCUTELLARIA LATERIFLORA contains SCUTELLARIA LATERIFLORA WHOLE. It is a pellet taken oral. Consult your doctor for specific uses.

Is SCUTELLARIA LATERIFLORA a controlled substance?

SCUTELLARIA LATERIFLORA is not classified as a controlled substance by the DEA.

What is the generic name for SCUTELLARIA LATERIFLORA?

The generic name for SCUTELLARIA LATERIFLORA is SCUTELLARIA LATERIFLORA WHOLE. There are no other listed brand versions of SCUTELLARIA LATERIFLORA WHOLE.

What is the NDC code for SCUTELLARIA LATERIFLORA 200 [kp_C]/200[kp_C]?

The NDC (National Drug Code) for SCUTELLARIA LATERIFLORA 200 [kp_C]/200[kp_C] is 0220-4600, listed by Boiron.

Product NDC

0220-4600

Package NDC

0220-4600-41

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

Data from openFDA · Public domain (CC0 1.0)