SSANGGI TANG- ssanghwa extract liquid

SSANGGI TANG by

Drug Labeling and Warnings

SSANGGI TANG by is a Otc medication manufactured, distributed, or labeled by I World Pharmaceutical Co., Ltd., I World Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

PURPOSE

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SSANGGI TANG 
ssanghwa extract liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73442-0009
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) (PAEONIA LACTIFLORA ROOT - UNII:3Z3866YW6P)	PAEONIA LACTIFLORA ROOT	0.9785 g  in 100 mL
REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (REHMANNIA GLUTINOSA ROOT - UNII:1BEM3U6LQQ)	REHMANNIA GLUTINOSA ROOT	0.6745 g  in 100 mL
LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97) (LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT - UNII:RR83T99U97)	LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT	0.627 g  in 100 mL
ASTRAGALUS GUMMIFER ROOT (UNII: 10T15Y9F0M) (ASTRAGALUS GUMMIFER ROOT - UNII:10T15Y9F0M)	ASTRAGALUS GUMMIFER ROOT	0.4845 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FRUCTOSE (UNII: 6YSS42VSEV)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73442-0009-1	80 mL in 1 POUCH; Type 0: Not a Combination Product	10/08/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/08/2019

Labeler - I World Pharmaceutical Co., Ltd. (688222857)

Registrant - I World Pharmaceutical Co., Ltd. (688222857)

Establishment
Name	Address	ID/FEI	Business Operations
I World Pharmaceutical Co., Ltd		688222857	manufacture(73442-0009)