CHEONGWIDAN-F- dry ginger, cinnamon bark, mentha herb pill

CHEONGWIDAN-F by

Drug Labeling and Warnings

CHEONGWIDAN-F by is a Otc medication manufactured, distributed, or labeled by Lydia Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Dry Ginger 100mg

CinnamonBark 100mg

Mentha Herb 100mg

INACTIVE INGREDIENT

Hawthorn Fruit, Gambir, Corn Starch, Sodium benzoate

PURPOSE

■Dyspepsia, Anorexia, Stomach bloating, Overeating, nausea, Vomit

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Directions

■adult and children 15 years of age and older: 1 dosage unit (20 pills) once, three times a day before or after meals.

■children 11 to 14 years of age: 2/3 of the adult capacity.

■children 8 to 10 years of age: 1/2 of the adult capacity.

WARNINGS

When using this product

■Do not use infants and toddlers under the age of seven.

■Do not use it for more than 1 month unless the symptoms improve.

■Do not change it to another container to prevent misuse and preserve quality.

■To keep the prescribed usage and capacity.

Ask a doctor before use if you take other medication.

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

Keep out of reach of children, In case of overdose, get medical help or contact a poison control center right away

DOSAGE & ADMINISTRATION

for oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CHEONGWIDAN-F 
dry ginger, cinnamon bark, mentha herb pill

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72988-0053
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ)	GINGER	100 mg  in 20
CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB)	CINNAMON	100 mg  in 20

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
MENTHA ARVENSIS TOP (UNII: 8J5Y2F7A5X)

Product Characteristics
Color	black	Score	no score
Shape	ROUND	Size	2mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72988-0053-1	120 in 1 PACKAGE	02/01/2025
1		20 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/01/2025

Labeler - Lydia Co., Ltd. (695735569)

Registrant - Lydia Co., Ltd. (695735569)

Establishment
Name	Address	ID/FEI	Business Operations
Lydia Co., Ltd.		695735569	manufacture(72988-0053) , label(72988-0053)