NDC 33261-039 Non-habit Forming Stool Softener
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-039 - Non-habit Forming Stool Softener
Product Characteristics
Product Packages
NDC Code 33261-039-00
Package Description: 100 CAPSULE, LIQUID FILLED in 1 BOTTLE
NDC Code 33261-039-02
Package Description: 120 CAPSULE, LIQUID FILLED in 1 BOTTLE
NDC Code 33261-039-10
Package Description: 10 CAPSULE, LIQUID FILLED in 1 BOTTLE
NDC Code 33261-039-20
Package Description: 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
NDC Code 33261-039-30
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE
NDC Code 33261-039-60
Package Description: 60 CAPSULE, LIQUID FILLED in 1 BOTTLE
NDC Code 33261-039-90
Package Description: 90 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Details
What is NDC 33261-039?
What are the uses for Non-habit Forming Stool Softener?
Which are Non-habit Forming Stool Softener UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
Which are Non-habit Forming Stool Softener 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:
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Non-habit Forming Stool Softener?
- RxCUI: 1115005 - docusate sodium 100 MG Oral Capsule
- RxCUI: 1115005 - DOSS Sodium 100 MG Oral Capsule
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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".