NDC 63868-603 Quality Choice Itch Relief

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:
63868-603
Proprietary Name:
Quality Choice Itch Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chain Drug Marketing Association Inc.
Labeler Code:
63868
Start Marketing Date: [9]
07-15-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63868-603-28

Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE

Product Details

What is NDC 63868-603?

The NDC code 63868-603 is assigned by the FDA to the product Quality Choice Itch Relief which is product labeled by Chain Drug Marketing Association Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63868-603-28 1 tube in 1 carton / 28 g in 1 tube. 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 Quality Choice Itch Relief?

Directionsfor itching of skin irritation, inflammation, and rashes:adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctorfor external anal and genital itching, adults:when practical, clean the affected area with mild soap and warm water and rinse thoroughlygently dry by patting or blotting with toilet tissue or a soft cloth before applyingapply to affected area not more than 3 to 4 times dailychildren under 12 years of age: ask a doctor

Which are Quality Choice Itch Relief UNII Codes?

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

Which are Quality Choice Itch Relief 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".