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  4. NDC Product Code: 63868-951 Quality Choice Hemorrhoidal

NDC 63868-951 Quality Choice Hemorrhoidal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63868-951?
  4. Quality Choice Hemorrhoidal Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63868-951
Proprietary Name:
Quality Choice Hemorrhoidal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chain Drug Marketing Association Inc
Labeler Code:
63868
Product Label ID:
8db1cff7-337f-4ed3-a4de-2d392eb908c6
Start Marketing Date: [9]
03-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63868-951-57

Package Description: 1 TUBE in 1 CARTON / 57 g in 1 TUBE

Product Details

What is NDC 63868-951?

The NDC code 63868-951 is assigned by the FDA to the product Quality Choice Hemorrhoidal 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 63868-951-57 1 tube in 1 carton / 57 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 Hemorrhoidal?

Directionschildren under 12 years of age: ask a doctor adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe gently dry by patting or blotting with a tissue or a soft cloth before applying when first opening tube, remove foil seal for intrarectal use: remove protective cover form applicator and attach to tube lubricate applicator well, then gently insert applicator into the rectum thoroughly clean applicator and replace protective cover after each use apply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement also apply ointment to external area

Which are Quality Choice Hemorrhoidal UNII Codes?

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

Which are Quality Choice Hemorrhoidal 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:

What is the NDC to RxNorm Crosswalk for Quality Choice Hemorrhoidal?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1544968 - mineral oil 14 % / petrolatum 71.9 % / phenylephrine HCl 0.25 % / shark liver oil preparation 3 % Rectal Ointment
  • RxCUI: 1544968 - mineral oil 0.14 MG/MG / petrolatum 0.719 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG / shark liver oil 0.03 MG/MG Rectal Ointment

* Please review the disclaimer below.

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".