NDC 61715-129 Fiber Therapy Regular Flavor

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61715-129
Proprietary Name:
Fiber Therapy Regular Flavor
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kinray Llc
Labeler Code:
61715
Start Marketing Date: [9]
09-28-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61715-129-13

Package Description: 283 g in 1 BOX

Product Details

What is NDC 61715-129?

The NDC code 61715-129 is assigned by the FDA to the product Fiber Therapy Regular Flavor which is product labeled by Kinray Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61715-129-13 283 g in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Fiber Therapy Regular Flavor?

Mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid. Taking this product with enough liquid may cause choking. Do not take if you have difficulty in swallowing. See choking warnings. Stir briskly and drink promptly. if mixture thickens, add more liquid and stir.LAXATIVE USEDIETARY SUPPLEMENT FIBER USEAdults 12 years & older1 rounded teaspoon (5.4 g) in 8 oz. of liquid at the first sign of irregularity. Can be taken up to 3 times daily1 rounded teaspoon (5.4 g) in 8 oz. of liquid 3 times daily. Children 6 years to under 12 years1/2 the adult dose in 8 oz. of liquid, up to 3 times dailyconsult a doctor Children under 6 yearsconsult a doctorconsult a doctor1.Put one dose into an empty glass2.Mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid.3.Taking this product without enough liquid may cause choking. See choking warining.4.Stir briskly and drink immediately. If mixture thickens, add more liquid and stir. An additional glass of liquid is recommended.Bulk forming fibers like psyllium 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 increase fiber intake, you may experience changes in bowel habits or minor bloating.New Users: Your doctor can recommend the right dosage of this product to best meet your needs. In general, start by taking one dose a day. Gradually increase to three doses per day, if needed or recommeded by your doctor.

Which are Fiber Therapy Regular Flavor UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Fiber Therapy Regular Flavor 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:

What is the NDC to RxNorm Crosswalk for Fiber Therapy Regular Flavor?

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:

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Product Footnotes

[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".