Ssanggi Tang Liquid
FDA Label NDC 73442-0009

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 Ssanggi Tang (NDC 73442-0009). 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

ssanghwa extract (peony root, rehmannia root, cnidium rhizome, astragalus root, angelica gias root, cinnamon bark, licorice, raw ginger, jujube)

Otc - Purpose

for cure fatigue, physical weakness, and illness such as cold sweats

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

take 1 pouch 3 times a day

Warnings

do not intake if the product is found to have expired or corrupted

when using this product be aware that the contents may flow when opening

stop use and ask a doctor if you have certain body types and allergies, it can cause a severe allergic reaction

Inactive Ingredient

water, liquid fructose

Dosage & Administration

For oral use only

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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