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NDC 71335-2693 Stimulant Laxative Plus Stool Softener

Docusate Sodium 50 Mg And Sennosides 8.6 Mg Tablet, Film Coated Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 71335-2693?
  5. Stimulant Laxative Plus Stool Softener Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 71335-2693 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
71335-2693
Proprietary Name:
Stimulant Laxative Plus Stool Softener
Non-Proprietary Name: [1]
Docusate Sodium 50 Mg And Sennosides 8.6 Mg
Substance Name: [2]
Docusate Sodium; Sennosides
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Bryant Ranch Prepack
Labeler Code:
71335
Product Label ID:
12f613e4-c919-4cc4-a445-eb30039ae45f
FDA Application Number: [6]
M007
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
10-22-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
PH32
Score:
1

Code Structure Chart

Product Details

What is NDC 71335-2693?

The NDC code 71335-2693 is assigned by the FDA to the product Stimulant Laxative Plus Stool Softener which is a human over the counter drug product labeled by Bryant Ranch Prepack. The generic name of Stimulant Laxative Plus Stool Softener is docusate sodium 50 mg and sennosides 8.6 mg. The product's dosage form is tablet, film coated and is administered via oral form. The product is distributed in 9 packages with assigned NDC codes 71335-2693-1 30 tablet, film coated in 1 bottle, plastic , 71335-2693-2 120 tablet, film coated in 1 bottle, plastic , 71335-2693-3 60 tablet, film coated in 1 bottle, plastic , 71335-2693-4 90 tablet, film coated in 1 bottle, plastic , 71335-2693-5 100 tablet, film coated in 1 bottle, plastic , 71335-2693-6 28 tablet, film coated in 1 bottle, plastic , 71335-2693-7 56 tablet, film coated in 1 bottle, plastic , 71335-2693-8 14 tablet, film coated in 1 bottle, plastic , 71335-2693-9 20 tablet, film coated in 1 bottle, plastic . 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 Stimulant Laxative Plus Stool Softener?

Take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided dosesadults and children 12 years and overtake 2-4 tablets dailychildren 6 to under 12 years of agetake 1-2 tablets dailychildren 2 to under 6 years of agetake upto 1 tablet dailychildren under 2 ask a doctor

What are Stimulant Laxative Plus Stool Softener Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • DOCUSATE SODIUM 50 mg/1 - All-purpose surfactant, wetting agent, and solubilizer used in the drug, cosmetics, and food industries. It has also been used in laxatives and as cerumenolytics. It is usually administered as either the calcium, potassium, or sodium salt.
  • SENNOSIDES 8.6 mg/1 - Medications derived from SENNA EXTRACT that are used to treat CONSTIPATION.

Which are Stimulant Laxative Plus Stool Softener UNII Codes?

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

Which are Stimulant Laxative Plus Stool Softener 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:

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

[6] 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.

[8] 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.

[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, 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".