Label: YOUNGGAKSAN- apricot kernel, powdered glycyrrhiza, powdered platycodon root, powdered senega powder
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Contains inactivated NDC Code(s)
NDC Code(s): 72988-0019-1 - Packager: LYDIA Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 8, 2019
If you are a consumer or patient please visit this version.
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- ACTIVE INGREDIENT
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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
- INDICATIONS & USAGE
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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
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YOUNGGAKSAN
apricot kernel, powdered glycyrrhiza, powdered platycodon root, powdered senega powderProduct 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)
