NDC 16480-002 Chan Yat Hing She Kun Wool Lok Medicated Oil

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:
16480-002
Proprietary Name:
Chan Yat Hing She Kun Wool Lok Medicated Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
16480
Start Marketing Date: [9]
12-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Code Structure Chart

Product Details

What is NDC 16480-002?

The NDC code 16480-002 is assigned by the FDA to the product Chan Yat Hing She Kun Wool Lok Medicated Oil which is product labeled by Chan Yat Hing Medicine Factory. The product's dosage form is . The product is distributed in a single package with assigned NDC code 16480-002-02 1 bottle, glass in 1 carton / 38 ml in 1 bottle, glass (16480-002-01). 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 Chan Yat Hing She Kun Wool Lok Medicated Oil?

Adults and children 2 years of age and older: apply 3 to 4 drops of medicated oil to the affected area 1 to 2 times daily. Children under 2 years of age: Do not use, consult your physician. Apply 3 to 4 drops of medicated oil to the affected area 1 to 2 times daily.

Which are Chan Yat Hing She Kun Wool Lok Medicated Oil UNII Codes?

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

Which are Chan Yat Hing She Kun Wool Lok Medicated Oil 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".