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  4. NDC Product Code: 63922-222 Sun Moon Star Pain Relieving

NDC 63922-222 Sun Moon Star Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63922-222?
  4. Sun Moon Star Pain Relieving Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63922-222
Proprietary Name:
Sun Moon Star Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kingsway Trading
Labeler Code:
63922
Product Label ID:
763c20db-ab44-4683-ab6f-e2bde735880a
Start Marketing Date: [9]
08-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 63922-222?

The NDC code 63922-222 is assigned by the FDA to the product Sun Moon Star Pain Relieving which is product labeled by Kingsway Trading. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63922-222-01 5 patch 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 Sun Moon Star Pain Relieving?

This product is used as External Analgesic. For the temporary relief of minor pains and aches of muscles and joints  associated with:simple backachearthritisstrainsbruisessprains

Which are Sun Moon Star Pain Relieving UNII Codes?

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

Which are Sun Moon Star Pain Relieving 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".