NDC 71335-1075 Fiber Caplets
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71335 - Bryant Ranch Prepack
- 71335-1075 - Fiber Caplets
Product Characteristics
Product Packages
NDC Code 71335-1075-1
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 71335-1075-2
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 71335-1075-3
Package Description: 120 TABLET in 1 BOTTLE
Product Details
What is NDC 71335-1075?
What are the uses for Fiber Caplets?
Which are Fiber Caplets UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM POLYCARBOPHIL (UNII: 8F049NKY49)
- POLYCARBOPHIL (UNII: W25LM17A4W) (Active Moiety)
Which are Fiber Caplets 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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARAMEL (UNII: T9D99G2B1R)
What is the NDC to RxNorm Crosswalk for Fiber Caplets?
- RxCUI: 308934 - calcium polycarbophil 625 MG Oral Tablet
- RxCUI: 308934 - calcium polycarbophil 625 MG (as polycarbophil 500 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".