Drugplain

Eucalyptus Globulus 500 [hp_C]/1

Eucalyptus Globulus · PELLET · Hahnemann Laboratories, INC.

No Recall History
Plain English

Eucalyptus Globulus is a pellet containing eucalyptus globulus at 500 [hp_C]/1, taken oral. Manufactured by Hahnemann Laboratories, INC..

Key Facts

Brand Name
Eucalyptus Globulus
Generic Name
Eucalyptus Globulus
NDC Code (Product)
37662-0686
Manufacturer
Hahnemann Laboratories, INC.
Strength
500 [hp_C]/1
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
06/21/2022

Recall History

No Recall History

Side Effects Reported to FDA

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

chronic obstructive pulmonary disease3 reports
drug hypersensitivity3 reports
dyspnoea3 reports
lower respiratory tract infection3 reports
atrial fibrillation2 reports
brain natriuretic peptide increased2 reports
bronchospasm2 reports
cardiac disorder2 reports
chest discomfort2 reports
coronary artery disease2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses: See symptoms on front panel. Relieves wet and irritating cough *

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 Eucalyptus Globulus used for?

Eucalyptus Globulus contains Eucalyptus Globulus. It is a pellet taken oral. Consult your doctor for specific uses.

Is Eucalyptus Globulus a controlled substance?

Eucalyptus Globulus is not classified as a controlled substance by the DEA.

What is the generic name for Eucalyptus Globulus?

The generic name for Eucalyptus Globulus is Eucalyptus Globulus. There are 11 other brand versions of Eucalyptus Globulus.

What is the NDC code for Eucalyptus Globulus 500 [hp_C]/1?

The NDC (National Drug Code) for Eucalyptus Globulus 500 [hp_C]/1 is 37662-0686, listed by Hahnemann Laboratories, INC..