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NDC 63922-605 Kgs Allergy Soothing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63922-605?
  5. Kgs Allergy Soothing Uses
  6. Active Ingredients UNII Codes
  7. 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:
63922-605
Proprietary Name:
Kgs Allergy Soothing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kingsway
Labeler Code:
63922
Product Label ID:
0a205049-811f-4f66-ac29-cb2a7b4efbf0
Start Marketing Date: [9]
01-30-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CLEAR)
Shape:
CAPSULE (C48336)
Size(s):
20 MM
Score:
2

Code Structure Chart

Product Details

What is NDC 63922-605?

The NDC code 63922-605 is assigned by the FDA to the product Kgs Allergy Soothing which is product labeled by Kingsway. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63922-605-01 1 blister pack in 1 box / 12 capsule, delayed release pellets in 1 blister pack (63922-605-12). 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 Kgs Allergy Soothing?

■ do not take more than directed (see Liver warning)adults and children 12 years of age and over■ take 2 caplets every 4 hours. ■swallow whole-do not crush, chew dissolve ■ do not take more than 12 capsules in 24 hours. ■ children under 12 years ask a doctor

Which are Kgs Allergy Soothing UNII Codes?

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

Which are Kgs Allergy Soothing 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".