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  4. NDC Product Code: 11822-4600 Rite Aid Fast Relief Laxative

NDC 11822-4600 Rite Aid Fast Relief Laxative

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 11822-4600?
  5. Rite Aid Fast Relief Laxative Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11822-4600
Proprietary Name:
Rite Aid Fast Relief Laxative
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid Pharmacy
Labeler Code:
11822
Product Label ID:
6d4770b6-f3c4-4cfb-8069-8e9cdceabc96
Start Marketing Date: [9]
10-01-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
BULLET (C48335)
Size(s):
32 MM

Code Structure Chart

Product Details

What is NDC 11822-4600?

The NDC code 11822-4600 is assigned by the FDA to the product Rite Aid Fast Relief Laxative which is product labeled by Rite Aid Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-4600-9 2 blister pack in 1 package / 40 mg in 1 blister pack (11822-4600-8). 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 Rite Aid Fast Relief Laxative?

Adults and children 12 years of age and older                 One suppository once daily Children 6 to 12 years                                                  1/2 suppository once daily                    Children under 6                                                          Ask doctor-Detach one suppository from the strip and remove from foil - Carefully insert one suppositry well into the rectum-Do not use more than once per day

Which are Rite Aid Fast Relief Laxative UNII Codes?

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

Which are Rite Aid Fast Relief Laxative 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 Rite Aid Fast Relief Laxative?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

* Please review the disclaimer below.

Patient Education

Bisacodyl Rectal


Rectal bisacodyl is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Bisacodyl is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
[Learn More]


* 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".