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  4. NDC Product Code: 0363-1760 Walgreens Maximum Strength Hemorrhoidal

NDC 0363-1760 Walgreens Maximum Strength Hemorrhoidal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0363-1760?
  4. Walgreens Maximum Strength 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:
0363-1760
Proprietary Name:
Walgreens Maximum Strength Hemorrhoidal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Company
Labeler Code:
0363
Product Label ID:
9191522e-f1d3-4922-8710-9827f78a823d
Start Marketing Date: [9]
02-25-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-1760-26

Package Description: 1 TUBE in 1 BOX / 26 g in 1 TUBE

Product Details

What is NDC 0363-1760?

The NDC code 0363-1760 is assigned by the FDA to the product Walgreens Maximum Strength Hemorrhoidal which is product labeled by Walgreen Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-1760-26 1 tube in 1 box / 26 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 Walgreens Maximum Strength Hemorrhoidal?

Directionsadults: 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 creamwhen first opening the tube, puncture foil seal with top end of capapply externally or in the lower portion of the anal canal onlyapply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movementfor application in the lower anal canal: remove cover from dispensing cap. Attach dispensing cap to tube. Lubricate dispensing cap well, then gently insert dispensing cap partway into the anusthoroughly cleanse dispensing cap after each use and replace coverchildren under 12 years of age: ask a doctor

Which are Walgreens Maximum Strength Hemorrhoidal UNII Codes?

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

Which are Walgreens Maximum Strength 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 Walgreens Maximum Strength 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: 1293649 - glycerin 14.4 % / phenylephrine HCl 0.25 % / pramoxine HCl 1 % / white petrolatum 15 % Rectal Cream
  • RxCUI: 1293649 - glycerin 144 MG/ML / petrolatum 150 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 15 % Rectal Cream

* 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".