YOUNGGAKSAN- apricot kernel, powdered glycyrrhiza, powdered platycodon root, powdered senega powder

YOUNGGAKSAN by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Apricot Kernel

Powdered Glycyrrhiza

Powdered Platycodon Root

Powdered Senega

PURPOSE

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

temporarily relieves:

cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants

the intensity of coughing

the impulse to cough to help you get to sleep

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Directions (take without water)

■ adult and children 15 years of age and older: 0.3g

■ children 7 to under 15 years of age: 0.2g three to six times a day

■ children 5 to under 7 years of age: 0.1g three to six times a day

■ children under 5 years of age: ask a doctor

WARNINGS

Ask a doctor before use if you have

persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema

cough accompanied by too much phlegm (mucus)

When using this product do not use more than directed

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

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.

INACTIVE INGREDIENT

cellulose, corn starch, magnesium stearate, sodium starch glycolate

DOSAGE & ADMINISTRATION

For oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YOUNGGAKSAN 
apricot kernel, powdered glycyrrhiza, powdered platycodon root, powdered senega powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72988-0019
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PLATYCODON GRANDIFLORUS ROOT (UNII: 2DF0NS0O2Z) (PLATYCODON GRANDIFLORUS ROOT - UNII:2DF0NS0O2Z)	PLATYCODON GRANDIFLORUS ROOT	11.7 mg  in 0.3 g
POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF)	POLYGALA SENEGA ROOT	0.5 mg  in 0.3 g
APRICOT KERNEL OIL (UNII: 54JB35T06A) (APRICOT KERNEL OIL - UNII:54JB35T06A)	APRICOT KERNEL OIL	0.83 mg  in 0.3 g
GLYCYRRHIZIN (UNII: 6FO62043WK) (GLYCYRRHIZIN - UNII:6FO62043WK)	GLYCYRRHIZIN	8.3 mg  in 0.3 g

Inactive Ingredients
Ingredient Name	Strength
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72988-0019-1	25 g in 1 JAR; 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 - LYDIA Co., Ltd (695735569)

Registrant - LYDIA Co., Ltd (695735569)

Establishment
Name	Address	ID/FEI	Business Operations
I World Pharmaceutical Co., Ltd		688222857	manufacture(72988-0019)

Establishment
Name	Address	ID/FEI	Business Operations
LYDIA Co., Ltd		695735569	label(72988-0019)