Drugplain

G-10 1 [hp_X]/mL

CEDRUS LIBANI WHOLE · SOLUTION · DNA Labs, Inc.

3 Recalls on Record
Plain English

G-10 is a solution containing cedrus libani whole at 1 [hp_X]/mL, taken sublingual. Manufactured by DNA Labs, Inc..

Key Facts

Brand Name
G-10
Generic Name
CEDRUS LIBANI WHOLE
NDC Code (Product)
58264-0373
Manufacturer
DNA Labs, Inc.
Strength
1 [hp_X]/mL
Dosage Form
SOLUTION
Route
SUBLINGUAL
Marketing Status
Marketing Start
01/01/1990

Recall History

3 Recalls on Record
Class II05/18/2022

Nephron Sterile Compounding Center LLC

Lack of Assurance of Sterility

TerminatedVoluntary: Firm initiated
Class II11/18/2016

Cantrell Drug Company

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

TerminatedVoluntary: Firm initiated
Class II11/09/2016

Sandoz Inc

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

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

drug ineffective1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS Respiratory and digestive irritations.

Dosage & Administration

SUGGESTED DOSAGE One dropper full twice daily.

Warnings

Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.

Frequently Asked Questions

What is G-10 used for?

G-10 contains CEDRUS LIBANI WHOLE. It is a solution taken sublingual. Consult your doctor for specific uses.

Is G-10 a controlled substance?

G-10 is not classified as a controlled substance by the DEA.

What is the generic name for G-10?

The generic name for G-10 is CEDRUS LIBANI WHOLE. There are no other listed brand versions of CEDRUS LIBANI WHOLE.

What is the NDC code for G-10 1 [hp_X]/mL?

The NDC (National Drug Code) for G-10 1 [hp_X]/mL is 58264-0373, listed by DNA Labs, Inc..

Product NDC

58264-0373

Package NDC

58264-0373-2

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

Data from openFDA · Public domain (CC0 1.0)