NDC 46122-384 Good Neighbor Pharmacy Gentle Laxative
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 46122 - Amerisourcebergen Drug Corp
- 46122-384 - Good Neighbor Pharmacy Gentle Laxative
Product Characteristics
Product Packages
NDC Code 46122-384-51
Package Description: 2 BLISTER PACK in 1 CARTON / 40 mg in 1 BLISTER PACK
Price per Unit: $0.26212 per EA
Product Details
What is NDC 46122-384?
What are the uses for Good Neighbor Pharmacy Gentle Laxative?
Which are Good Neighbor Pharmacy Gentle Laxative UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISACODYL (UNII: 10X0709Y6I)
- BISACODYL (UNII: 10X0709Y6I) (Active Moiety)
Which are Good Neighbor Pharmacy Gentle 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:
- FAT, HARD (UNII: 8334LX7S21)
What is the NDC to RxNorm Crosswalk for Good Neighbor Pharmacy Gentle Laxative?
- RxCUI: 198509 - bisacodyl 10 MG Rectal Suppository
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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.
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[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".