NDC 55910-402 Rexall Maximum Strength Hemorrhoidal

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:
55910-402
Proprietary Name:
Rexall Maximum Strength Hemorrhoidal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dolgencorp, Inc.
Labeler Code:
55910
Start Marketing Date: [9]
06-28-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 55910-402-03

Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 28 g in 1 TUBE, WITH APPLICATOR

Product Details

What is NDC 55910-402?

The NDC code 55910-402 is assigned by the FDA to the product Rexall Maximum Strength Hemorrhoidal which is product labeled by Dolgencorp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55910-402-03 1 tube, with applicator in 1 carton / 28 g in 1 tube, with applicator. 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 Rexall Maximum Strength Hemorrhoidal?

Uses- for temporary relief of pain, soreness and burning - helps relieve the local itching and discomfort associated with hemorrhoids - temporarily shrinks hemorrhoidal tissue - temporarily provides a coating for relief of anorectal discomforts - temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful Other information- store at 20 degrees - 25 degrees C (68 degrees - 77 degrees F)- for lot number and expiration date, see crimp of tube or see box

Which are Rexall Maximum Strength Hemorrhoidal UNII Codes?

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

Which are Rexall 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 Rexall 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

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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".