Thuja 30 [hp_C]/mL

Thuja Occidentalis · LIQUID · Energique, Inc.

1 Recall on Record

Plain English

Thuja is a liquid containing thuja occidentalis at 30 [hp_C]/mL, taken oral. Manufactured by Energique, Inc..

Key Facts

1 Recall on Record

Class II08/20/2021

Washington Homeopathic Products, Inc.

Out-of-specification test results obtained for identification testing based on HPTLC analysis.

TerminatedVoluntary: Firm initiated

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

agranulocytosis1 reports

drug ineffective1 reports

flatulence1 reports

haematochezia1 reports

irritability1 reports

treatment failure1 reports

Source: FDA Drug Label (SPL)For healthcare professionals

USE: Condition listed above or as directed by a physician.

DIRECTIONS: (adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

WARNINGS: Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Thuja contains Thuja Occidentalis. It is a liquid taken oral. Consult your doctor for specific uses.

Thuja is not classified as a controlled substance by the DEA.

The generic name for Thuja is Thuja Occidentalis. There are 12 other brand versions of Thuja Occidentalis.

The NDC (National Drug Code) for Thuja 30 [hp_C]/mL is 44911-0156, listed by Energique, Inc..

Product NDC

44911-0156

Package NDC

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

Data from openFDA · Public domain (CC0 1.0)