Drugplain

Cuprum Oxydatum Nigrum 30 [hp_C]/1

Cuprum Oxydatum Nigrum · PELLET · Hahnemann Laboratories, INC.

No Recall History
Plain English

Cuprum Oxydatum Nigrum is an over-the-counter oral pellet used in homeopathic medicine. This product is taken by mouth and is available without a prescription.

Key Facts

Brand Name
Cuprum Oxydatum Nigrum
Generic Name
Cuprum Oxydatum Nigrum
NDC Code (Product)
37662-0659
Manufacturer
Hahnemann Laboratories, INC.
Strength
30 [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

drug ineffective377 reports
macular degeneration369 reports
nausea117 reports
weight decreased116 reports
pain114 reports
therapeutic product effect incomplete114 reports
chronic sinusitis112 reports
malaise112 reports
paraesthesia oral112 reports
pyrexia112 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses: See symptoms on front panel. Relieves nervousness in children *

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 Cuprum Oxydatum Nigrum used for?

Cuprum Oxydatum Nigrum is an over-the-counter oral pellet used in homeopathic medicine. This product is taken by mouth and is available without a prescription.

Is Cuprum Oxydatum Nigrum a controlled substance?

Cuprum Oxydatum Nigrum is not classified as a controlled substance by the DEA.

What is the generic name for Cuprum Oxydatum Nigrum?

The generic name for Cuprum Oxydatum Nigrum is Cuprum Oxydatum Nigrum. There are no other listed brand versions of Cuprum Oxydatum Nigrum.

What is the NDC code for Cuprum Oxydatum Nigrum 30 [hp_C]/1?

The NDC (National Drug Code) for Cuprum Oxydatum Nigrum 30 [hp_C]/1 is 37662-0659, listed by Hahnemann Laboratories, INC..

Product NDC

37662-0659

Package NDC

37662-0659-1

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

Data from openFDA · Public domain (CC0 1.0)