NDC 29485-6741 Dulcolax
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 29485-6741?
What are the uses for Dulcolax?
Which are Dulcolax UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISACODYL (UNII: 10X0709Y6I)
- BISACODYL (UNII: 10X0709Y6I) (Active Moiety)
Which are Dulcolax 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:
- ACACIA (UNII: 5C5403N26O)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CELLACEFATE (UNII: F2O5O2OI9F)
- STARCH, CORN (UNII: O8232NY3SJ)
- DIBUTYL PHTHALATE (UNII: 2286E5R2KE)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- KAOLIN (UNII: 24H4NWX5CO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SHELLAC (UNII: 46N107B71O)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WHITE WAX (UNII: 7G1J5DA97F)
- DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Dulcolax?
- RxCUI: 209613 - Dulcolax 5 MG Delayed Release Oral Tablet
- RxCUI: 209613 - bisacodyl 5 MG Delayed Release Oral Tablet [Dulcolax]
- RxCUI: 308753 - bisacodyl 5 MG Delayed Release Oral Tablet
- RxCUI: 308753 - bisacodyl 5 MG Enteric Coated Oral Tablet
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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".