NDC 51367-033 Shexiang Zhuanggu Gao

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:
51367-033
Proprietary Name:
Shexiang Zhuanggu Gao
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
International Nature Nutraceuticals
Labeler Code:
51367
Start Marketing Date: [9]
04-15-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51367-033-10

Package Description: 10 PLASTER in 1 BOX

Product Details

What is NDC 51367-033?

The NDC code 51367-033 is assigned by the FDA to the product Shexiang Zhuanggu Gao which is product labeled by International Nature Nutraceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51367-033-10 10 plaster in 1 box . 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 Shexiang Zhuanggu Gao?

Adults and Children 12 years of age and older: apply one or two plasters to affected area once a day, remove after 12 hoursChildren 2 to 12 years of age and adults with compromised health: use only the guidance of a doctorChildren under 2 years of age: do not use

Which are Shexiang Zhuanggu Gao UNII Codes?

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

Which are Shexiang Zhuanggu Gao 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".