NDC 70795-1010 Laxative

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:
70795-1010
Proprietary Name:
Laxative
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Graxcell Pharmaceutical, Llc
Labeler Code:
70795
Start Marketing Date: [9]
03-29-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 70795-1010-1

Package Description: 100 BLISTER PACK in 1 PACKAGE / 1 SUPPOSITORY in 1 BLISTER PACK

NDC Code 70795-1010-5

Package Description: 50 BLISTER PACK in 1 BOX / 1 SUPPOSITORY in 1 BLISTER PACK

NDC Code 70795-1010-8

Package Description: 8 BLISTER PACK in 1 BOX / 1 SUPPOSITORY in 1 BLISTER PACK

Product Details

What is NDC 70795-1010?

The NDC code 70795-1010 is assigned by the FDA to the product Laxative which is product labeled by Graxcell Pharmaceutical, Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 70795-1010-1 100 blister pack in 1 package / 1 suppository in 1 blister pack, 70795-1010-5 50 blister pack in 1 box / 1 suppository in 1 blister pack, 70795-1010-8 8 blister pack in 1 box / 1 suppository in 1 blister pack. 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 Laxative?

Detach one suppository from the strip and remove from foilCarefully insert one supoository well into the rectumDo not use more than once per day

Which are Laxative UNII Codes?

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

Which are 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 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:

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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]


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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".