RUTA GRAVEOLENS 1 [hp_X]/1

RUTA GRAVEOLENS · PELLET · Rxhomeo Private Limited d.b.a. Rxhomeo, Inc

1 Recall on Record

Plain English

RUTA GRAVEOLENS is a pellet containing ruta graveolens at 1 [hp_X]/1, taken oral. Manufactured by Rxhomeo Private Limited d.b.a. Rxhomeo, Inc.

Key Facts

Brand Name: RUTA GRAVEOLENS
Generic Name: RUTA GRAVEOLENS
NDC Code (Product): 15631-0379
Manufacturer: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Strength: 1 [hp_X]/1
Dosage Form: PELLET
Route: ORAL
Marketing Status
Marketing Start: 10/31/2015

Recall History

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

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses: See symptoms on front panel. Relieves eye strain due to computer use or artificial lights *

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 RUTA GRAVEOLENS used for?

RUTA GRAVEOLENS contains RUTA GRAVEOLENS. It is a pellet taken oral. Consult your doctor for specific uses.

Is RUTA GRAVEOLENS a controlled substance?

RUTA GRAVEOLENS is not classified as a controlled substance by the DEA.

What is the generic name for RUTA GRAVEOLENS?

The generic name for RUTA GRAVEOLENS is RUTA GRAVEOLENS. There are 11 other brand versions of RUTA GRAVEOLENS.

What is the NDC code for RUTA GRAVEOLENS 1 [hp_X]/1?

The NDC (National Drug Code) for RUTA GRAVEOLENS 1 [hp_X]/1 is 15631-0379, listed by Rxhomeo Private Limited d.b.a. Rxhomeo, Inc.

Product NDC

15631-0379

Package NDC

15631-0379-0

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

Data from openFDA · Public domain (CC0 1.0)