NDC 69676-0050 Genexa Senna Laxative


NDC Product Code 69676-0050

NDC CODE: 69676-0050

Proprietary Name: Genexa Senna Laxative What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Sennosides 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Sennosides are used to treat constipation. They may also be used to clean out the intestines before a bowel examination/surgery. Sennosides are known as stimulant laxatives. They work by keeping water in the intestines, which causes movement of the intestines.

Product Characteristics

BROWN (C48332)
Shape: ROUND (C48348)
10 MM
Score: 1

NDC Code Structure

  • 69676 - Genexa Inc.

NDC 69676-0050-5

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 50 TABLET in 1 BOTTLE, PLASTIC

NDC Product Information

Genexa Senna Laxative with NDC 69676-0050 is a a human over the counter drug product labeled by Genexa Inc.. The generic name of Genexa Senna Laxative is sennosides. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Genexa Inc.

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.

Genexa Senna Laxative 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.

  • SENNOSIDES 12 mg/1

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.
  • 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: Genexa Inc.
Labeler Code: 69676
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: 10-20-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Genexa Senna Laxative Product Label Images

Genexa Senna Laxative 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


Keep outer package for complete product informationDrug Facts

Bottle is safety sealed. DO NOT use if bottle seal is disturbed or missing.Patent Pending | Distributed by:Genexa Inc. Los Angeles, CA 90034genexa.comCertified Organic by SCS Global Services

Made in the USA with globally sourced ingredientsR-20200728NDC 69676-0050-5

Otc - Active Ingredient

Active ingredient
+ (in each tablet)
Sennosides 12 mg*Certified Organic

Otc - Purpose


Indications & Usage

  • Usesrelieves occasional constipation (irregularity)generally produces bowel movement in 6 to 12 hours



Otc - Do Not Use

  • Do not uselonger than one week, unless directed by a doctorwhen abdominal pain, nausea, or vomiting are present

Otc - Ask Doctor

Ask a doctor before use if you have noticed a sudden change in bowel habits that persists over a period of 2 weeks.

Otc - Ask Doctor/Pharmacist

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. Laxatives may affect how other drugs work.

Otc - Stop Use

Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may be signs of a serious conditon.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Dosage & Administration

DirectionsTake preferably at bedtime or as directed by a doctor.adults and children 12 years of age and over1 tablet once or twice dailychildren 6 to under 12 years of age1/2 tablet once or twice dailychildren under 6 years of ageask a doctor before use

Storage And Handling

Other informationstore between 20-25°C (68-77°F) in a dry place out of direct sunlight

Inactive Ingredient

Inactive ingredients organic rice bran extract, organic rice extract blend, sodium bicarbonate, organic tapioca dextrose, organic tapioca maltodextrin

Otc - Questions

Questions?1-855-436-3921Monday.-Fri. 7am - 6pm PST

* Please review the disclaimer below.