NDC 71291-0011 Stem Cell Extract Of Wild Mountain Ginseng

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Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71291-0011
Proprietary Name:
Stem Cell Extract Of Wild Mountain Ginseng
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
71291
Start Marketing Date: [9]
11-14-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 71291-0011?

The NDC code 71291-0011 is assigned by the FDA to the product Stem Cell Extract Of Wild Mountain Ginseng which is product labeled by Geolim Pharmaceutical Co., Ltd. (busan Branch). The product's dosage form is . The product is distributed in a single package with assigned NDC code 71291-0011-1 10 ml in 1 vial . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Stem Cell Extract Of Wild Mountain Ginseng?

- 5 - 100 ml (usually 10 ml) of the Wild Cultivated Ginseng Purified Pharmacopuncture is intravenous injection. • In case of a patient who has a serious illness after the treatment of a oriental medical doctor, administer 1 Oml once every 3 days or once a week for a general patient by intravenous injection. • In winter season, Wild Cultivated Ginseng Purified Pharmacopuncture injcetion temperature is 37.5 degrees, and gradually injected into for 3 minutes.

Which are Stem Cell Extract Of Wild Mountain Ginseng UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Stem Cell Extract Of Wild Mountain Ginseng Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".