CHUNGWIDAN-F- cinnamon, ginger liquid

CHUNGWIDAN-F by

Drug Labeling and Warnings

CHUNGWIDAN-F by is a Otc medication manufactured, distributed, or labeled by Han Kook Shin Yak Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Cinnamon 500 mg Ginger 300 mg

Digestive aid

This Oriental medicine is made from a combination of ingredients traditionally used to help relieve symptoms associated with indigestion: ■ appetite loss ■ abdominal bloating ■ dyspepsia ■ nausea ■ vomiting

Warnings Stop use and ask a doctor if ■ symptoms get worse

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions ■ Shake well before use ■ Up to three bottles per day may be consumed. One bottle (30mL) after each meal with no less than 4 hours between each consumption. ■ For ages 10-14 : 20mL ■ For ages 7-9: 10mL ■ For ages 4-6: 7.5mL ■ For ages 2-4: 6mL

Black atractylodes rhizome, Cloves, Crataegi fructus, Geranium herb, Hardy orange fruit, Lindera root, Mint, Nutmeg, Purified water, Sun-dried tangerine peel, Syrup extract, Sugar, Sodium benzoate, Sorbitol solution, Sodium Citrate Hydrate.

CHUNGWIDAN-F

INGREDIENTS AND APPEARANCE

CHUNGWIDAN-F 
cinnamon, ginger liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53153-103
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB)	CINNAMON	500 mg  in 30 mL
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ)	GINGER	300 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
NUTMEG (UNII: AEE24M3MQ9)
MINT (UNII: FV98Z8GITP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53153-103-03	10 in 1 CARTON	12/18/2019
1	NDC: 53153-103-02	3 in 1 BOX
1	NDC: 53153-103-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/18/2019

Labeler - Han Kook Shin Yak Pharmaceutical Co., Ltd. (689277536)

Registrant - Han Kook Shin Yak Pharmaceutical Co., Ltd. (689277536)

Establishment
Name	Address	ID/FEI	Business Operations
Han Kook Shin Yak Pharmaceutical Co., Ltd.		689277536	manufacture(53153-103)