NDC 63868-208 Hemorrhoidal
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - Chain Drug Marketing Association, Inc.
- 63868-208 - Hemorrhoidal
Product Packages
NDC Code 63868-208-12
Package Description: 12 BLISTER PACK in 1 BOX / 1 SUPPOSITORY in 1 BLISTER PACK
Price per Unit: $0.22018 per EA
NDC Code 63868-208-24
Package Description: 24 BLISTER PACK in 1 BOX / 1 SUPPOSITORY in 1 BLISTER PACK
Product Details
What is NDC 63868-208?
What are the uses for Hemorrhoidal?
Which are Hemorrhoidal UNII Codes?
The UNII codes for the active ingredients in this product are:
- COCOA BUTTER (UNII: 512OYT1CRR)
- COCOA BUTTER (UNII: 512OYT1CRR) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Hemorrhoidal?
- RxCUI: 1438497 - cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository
- RxCUI: 1438497 - cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository
* Please review the disclaimer below.
[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".