NDC 54162-195 Docusate Sodium Liquid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54162 - Geritrex Llc
- 54162-195 - Docusate Sodium Liquid
Product Packages
NDC Code 54162-195-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54162-195?
What are the uses for Docusate Sodium Liquid?
Which are Docusate Sodium Liquid UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
Which are Docusate Sodium Liquid 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- WATER (UNII: 059QF0KO0R)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Docusate Sodium Liquid?
- RxCUI: 1248119 - docusate sodium 50 MG in 5 mL Oral Suspension
- RxCUI: 1248119 - docusate sodium 10 MG/ML Oral Suspension
- RxCUI: 1248119 - docusate sodium 100 MG per 10 ML Oral Suspension
- RxCUI: 1248119 - docusate sodium 150 MG per 15 ML Oral Suspension
- RxCUI: 1248119 - docusate sodium 50 MG per 5 ML Oral Suspension
* 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".