NDC 73305-0001 Shineph

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73305-0001
Proprietary Name:
Shineph
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
73305
Start Marketing Date: [9]
08-17-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 73305-0001?

The NDC code 73305-0001 is assigned by the FDA to the product Shineph which is product labeled by Ch Bio Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73305-0001-1 1.5 g in 1 applicator . 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 Shineph?

Hold the handle in the middle, and pull the shorter cap to the direction of arrow to separate as shown in the picture.Pull the other cap to the direction of arrow to separatePush the piston at the external genital slowly and absorb all the contents.Lightly rinse with water.

Which are Shineph UNII Codes?

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

  • LITHOSPERMUM OFFICINALE ROOT (UNII: VOD5H80TXG)
  • LITHOSPERMUM OFFICINALE ROOT (UNII: VOD5H80TXG) (Active Moiety)
  • ARTEMISIA PRINCEPS LEAF OIL (UNII: F9S1101A2V)
  • ARTEMISIA PRINCEPS LEAF OIL (UNII: F9S1101A2V) (Active Moiety)
  • MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
  • MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) (Active Moiety)
  • CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
  • CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB) (Active Moiety)

Which are Shineph 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".