NDC 17856-0771 Docu Liquid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-0771 - Docu Liquid
Product Characteristics
Product Packages
NDC Code 17856-0771-1
Package Description: 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 25 mL in 1 CUP, UNIT-DOSE
NDC Code 17856-0771-2
Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE
Product Details
What is NDC 17856-0771?
What are the uses for Docu Liquid?
Which are Docu 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 Docu 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:
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- WATER (UNII: 059QF0KO0R)
- POLOXAMER 181 (UNII: 09Y8E6164A)
What is the NDC to RxNorm Crosswalk for Docu 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
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Patient Education
Stool Softeners
Stool softeners are used on a short-term basis to relieve constipation by people who should avoid straining during bowel movements because of heart conditions, hemorrhoids, and other problems. They work by softening stools to make them easier to pass.
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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".