Cvs Health Natural Daily Fiber Sugar Free
NDC 59779-875
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
Cvs Health Natural Daily Fiber Sugar Free is a OTC MONOGRAPH NOT FINAL-approved product labeled by Cvs Pharmacy,inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a brown product. This product entry covers the primary NDC 59779-875 and 3 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
59779-875
Proprietary Name:
Cvs Health Natural Daily Fiber Sugar Free Natural Fiber
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
59779
Product Label ID:
FDA Application Number: [6]
part334
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Marketing Timeline
Start Marketing Date: [9]
08-17-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Product Characteristics
Color(s):
BROWN (C48332 - LIGHT YELLOWISH)
Flavor(s):
Code Structure Chart
Product Details
What is NDC 59779-875?
The NDC code 59779-875 is assigned by the FDA to the product Cvs Health Natural Daily Fiber Sugar Free Natural Fiber. This pharmaceutical product is labeled by Cvs Pharmacy,inc. and is currently categorized as listed product. In terms of distribution, this product is available in 3 different package configurations. The associated package NDC(s) include: 59779-875-14, 59779-875-48, 59779-875-80. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Put one dose into an empty glass. Mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid. Taking this product without enough liquid may cause choking. See choking warning. Stir briskly and drink promptly. If mixture thickens, add more liquid and stir.Adults 12 years & older:1 rounded TEASPOON in 8 oz of liquid at the first sign of irregularity. Can be taken up to 3 times daily. Generally produces effect in 12-72 hours.6 – 11 yrs :½ adult dose in 8 oz of liquid, up to 3 times dailyUnder 6 yrs:Consult a doctorBulk forming fibers like psyllium husk may affect how well other medicines work. If you are taking a prescription medicine by mouth, take this product at least 2 hours before or 2 hours after the prescribed medicine. As your body adjusts to increased fiber intake, you may experience changes in bowel habits or minor bloating.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- PSYLLIUM HUSK (UNII: 0SHO53407G)
- PSYLLIUM HUSK (UNII: 0SHO53407G) (Active Moiety)
Which are the Inactive Ingredients associated 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:
- ASPARTAME (UNII: Z0H242BBR1)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for this product?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
- RxCUI: 824586 - psyllium 3.4 GM Powder for Oral Suspension
- RxCUI: 824586 - psyllium 3400 MG Powder for Oral Suspension
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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
