NDC 71335-1075 Fiber Caplets

Calcium Polycarbophil

NDC Product Code 71335-1075

NDC 71335-1075-1

Package Description: 30 TABLET in 1 BOTTLE

NDC 71335-1075-2

Package Description: 60 TABLET in 1 BOTTLE

NDC 71335-1075-3

Package Description: 120 TABLET in 1 BOTTLE

NDC Product Information

Fiber Caplets with NDC 71335-1075 is a a human over the counter drug product labeled by Bryant Ranch Prepack. The generic name of Fiber Caplets is calcium polycarbophil. The product's dosage form is tablet and is administered via oral form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 308934.

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Fiber Caplets Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bryant Ranch Prepack
Labeler Code: 71335
FDA Application Number: part334 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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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.

Start Marketing Date: 06-01-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Fiber Caplets Product Label Images

Fiber Caplets Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (In Each Caplet)

Calcium polycarbophil 625 mg equivalent to 500 mg polycarbophil


Bulk-forming laxative


  • Relieves occasional constipationthis product generally produces bowel movement in 12 to 72 hours


Choking: Taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting, or difficulty in swallowing or breathing after taking this product, seek immediate medical attention.

Ask A Doctor Before Use If You Have

  • Abdominal pain, nausea or vomitingdifficulty in swallowinga sudden change in bowel habits that persists over a period of 2 weeks

Ask A Doctor Or Pharmacist Before Use If You Are

Taking any other drug. Take this product 2 or more hours before or after other drugs. All laxatives may affect how other drugs work.

When Using This Product

  • Do not use for more than 7 days unless directed by a doctordo not take more than 8 caplets in a 24 hour period unless directed by a doctor.

Stop Use And Ask A Doctor If

  • You experience chest pain, abdominal pain, nausea, vomiting, difficulty in breathing or swallowingyou fail to have a bowel movement after use or have rectal bleeding. These could be signs of a serious condition.

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center immediately.


  • Take this product (child or adult dose) with a full glass of water (8 oz.) or other fluid. Taking this product without enough liquid may cause choking. See choking warning.dosage will vary according to diet, excercise, previous laxative use or severity of constipation.continued use for 1 or 3 days is normally required to provide full benefit. adults and children 12 years and over                                                                  2 caplets, 1 to 4 times a day                                             Children under 12 years  ask a doctor

Other Information

  • Each caplet contains: calcium 135mgdo not use if printed seal under cap is torn or missingstore at room temperatureprotect contents from moisture

Inactive Ingredients

Calcium carbonate, caramel, colloidal silicon dioxide, crospovidone, hydroxypropyl methylcellulose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium lauryl sulfate

How Supplied

Product: 71335-1075NDC: 71335-1075-1 30 TABLET in a BOTTLENDC: 71335-1075-2 60 TABLET in a BOTTLENDC: 71335-1075-3 120 TABLET in a BOTTLE

* Please review the disclaimer below.