NDC 70518-1590 Senna Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70518 - Remedyrepack Inc.
- 70518-1590 - Senna Plus
Product Characteristics
Product Packages
NDC Code 70518-1590-0
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 70518-1590?
What are the uses for Senna Plus?
Which are Senna Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- SENNOSIDES (UNII: 3FYP5M0IJX)
- SENNOSIDES (UNII: 3FYP5M0IJX) (Active Moiety)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
Which are Senna Plus 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Senna Plus?
- RxCUI: 998740 - sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet
- RxCUI: 998740 - docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet
- RxCUI: 998740 - DOSS Sodium 50 MG / sennosides, USP 8.6 MG 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".