Socheongryong Tang Extract Granule
FDA Label NDC 73442-0012

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by I World Pharmaceutical Co., Ltd. for the product Socheongryong Tang Extract (NDC 73442-0012). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Ginger(KP)
Chlorpheniramine maleate
Dextromethorphan Hydrobromide

Otc - Purpose

bronchitis, bronchial asthma, runny nose, phlegm cough, rhinitis

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

for adults take 1 pouch per intake, 3 times a day, before or between meals

Warnings

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

Dried Socheongryong Tang Ext(KHP), Pinellia Tuber(KP), Licorice(KP), Cinnamomum Branch(KHP), Ephedra Herb(KP), Peony Root(KP), Asiasari Radix(KP), Schisandra Fruit(KP)

Dosage & Administration

For oral use only

Package Label.Principal Display Panel

Label (Label)

Label (Label)

* Please review the disclaimer below.