Drugplain

AM-12 8 [hp_X]/mL

STRYCHNOS IGNATII WHOLE, FERROSOFERRIC PHOSPHATE, and SEPIA OFFICINALIS JUICE · SOLUTION · DNA Labs, Inc.

No Recall History
Plain English

AM-12 is a solution containing strychnos ignatii whole, ferrosoferric phosphate, and sepia officinalis juice at 8 [hp_X]/mL, taken sublingual. Manufactured by DNA Labs, Inc..

Key Facts

Brand Name
AM-12
Generic Name
STRYCHNOS IGNATII WHOLE, FERROSOFERRIC PHOSPHATE, and SEPIA OFFICINALIS JUICE
NDC Code (Product)
58264-0351
Manufacturer
DNA Labs, Inc.
Strength
8 [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

fall1 reports
hypoglycaemia1 reports
injury1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS Regulates energy flow in the bladder meridian.

Dosage & Administration

SUGGESTED DOSAGE 5 to 10 drops twice a day, meridian energy excess 1 to 5 drops t.i.d, meridian lacking in energy 10 to 20 drops t.i.d.

Warnings

Warnings Use only if cap seal is unbroken. As with drugs if you are pregnant or nursing a baby seek professional advice before using this product. Keep this and all medication out of the reach of children.

Frequently Asked Questions

What is AM-12 used for?

AM-12 contains STRYCHNOS IGNATII WHOLE, FERROSOFERRIC PHOSPHATE, and SEPIA OFFICINALIS JUICE. It is a solution taken sublingual. Consult your doctor for specific uses.

Is AM-12 a controlled substance?

AM-12 is not classified as a controlled substance by the DEA.

What is the generic name for AM-12?

The generic name for AM-12 is STRYCHNOS IGNATII WHOLE, FERROSOFERRIC PHOSPHATE, and SEPIA OFFICINALIS JUICE. There are no other listed brand versions of STRYCHNOS IGNATII WHOLE, FERROSOFERRIC PHOSPHATE, and SEPIA OFFICINALIS JUICE.

What is the NDC code for AM-12 8 [hp_X]/mL?

The NDC (National Drug Code) for AM-12 8 [hp_X]/mL is 58264-0351, listed by DNA Labs, Inc..

Product NDC

58264-0351

Package NDC

58264-0351-1

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

Data from openFDA · Public domain (CC0 1.0)