NDC 46084-111 Apj 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:
46084-111
Proprietary Name:
Apj Hemorrhoidal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A P J Laboratories Limited
Labeler Code:
46084
Start Marketing Date: [9]
07-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OFF WHITE)

Product Packages

NDC Code 46084-111-10

Package Description: 28 g in 1 TUBE

NDC Code 46084-111-20

Package Description: 57 g in 1 TUBE

Product Details

What is NDC 46084-111?

The NDC code 46084-111 is assigned by the FDA to the product Apj Hemorrhoidal which is product labeled by A P J Laboratories Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 46084-111-10 28 g in 1 tube , 46084-111-20 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 Apj Hemorrhoidal?

■ Helps relieve the local itching and discomfort associated with hemorrhoids.■ Temporarily shrinks hemorrhoidal tissue and relieves burning.■ Temporarily provides a coating for relief of anorectal discomforts.■ Temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful.

Which are Apj Hemorrhoidal UNII Codes?

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

Which are Apj 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:

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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".