G-22 1 [hp_X]/mL

LIGUSTRUM VULGARE WHOLE · SOLUTION · DNA Labs, Inc.

No Recall History

Plain English

G-22 is a solution containing ligustrum vulgare whole at 1 [hp_X]/mL, taken sublingual. Manufactured by DNA Labs, Inc..

Key Facts

Brand Name: G-22
Generic Name: LIGUSTRUM VULGARE WHOLE
NDC Code (Product): 58264-0385
Manufacturer: DNA Labs, Inc.
Strength: 1 [hp_X]/mL
Dosage Form: SOLUTION
Route: SUBLINGUAL
Marketing Status
Marketing Start: 01/01/1990

Recall History

No Recall History

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 Heavy menses.

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-22 used for?

G-22 contains LIGUSTRUM VULGARE WHOLE. It is a solution taken sublingual. Consult your doctor for specific uses.

Is G-22 a controlled substance?

G-22 is not classified as a controlled substance by the DEA.

What is the generic name for G-22?

The generic name for G-22 is LIGUSTRUM VULGARE WHOLE. There are no other listed brand versions of LIGUSTRUM VULGARE WHOLE.

What is the NDC code for G-22 1 [hp_X]/mL?

The NDC (National Drug Code) for G-22 1 [hp_X]/mL is 58264-0385, listed by DNA Labs, Inc..

Product NDC

58264-0385

Package NDC

58264-0385-2

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

Data from openFDA · Public domain (CC0 1.0)