NDC 73442-0005 Younggaksan

Apricot Kernel, Powdered Glycyrrhiza, Powdered Platycodon Root, Powdered Senega

NDC Product Code 73442-0005

NDC CODE: 73442-0005

Proprietary Name: Younggaksan What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Apricot Kernel, Powdered Glycyrrhiza, Powdered Platycodon Root, Powdered Senega What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 73442 - I World Pharmaceutical Co., Ltd.

NDC 73442-0005-1

Package Description: 25 g in 1 JAR

NDC Product Information

Younggaksan with NDC 73442-0005 is a a human over the counter drug product labeled by I World Pharmaceutical Co., Ltd.. The generic name of Younggaksan is apricot kernel, powdered glycyrrhiza, powdered platycodon root, powdered senega. The product's dosage form is powder and is administered via oral form.

Labeler Name: I World Pharmaceutical Co., Ltd.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Younggaksan Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • PLATYCODON GRANDIFLORUS ROOT 11.7 mg/.3g
  • POLYGALA SENEGA ROOT .5 mg/.3g
  • APRICOT KERNEL OIL .83 mg/.3g
  • GLYCYRRHIZIN 8.3 mg/.3g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • POWDERED CELLULOSE (UNII: SMD1X3XO9M)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: I World Pharmaceutical Co., Ltd.
Labeler Code: 73442
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-08-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Younggaksan Product Label Images

Younggaksan Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Apricot KernelPowdered Glycyrrhiza Powdered Platycodon Root Powdered Senega

Otc - Purpose

Helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productivetemporarily relieves:cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritantsthe intensity of coughingthe impulse to cough to help you get to sleep

Otc - 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 havepersistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysemacough accompanied by too much phlegm (mucus)When using this product do not use more than directedStop use and ask a doctor ifcough 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

* Please review the disclaimer below.