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OTC products · Product label record

Senokot drug information

STANDARDIZED SENNA
A-S Medication Solutions · ORAL

Product NDC: 50090-8045

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameSTANDARDIZED SENNA
Labeler / manufacturerA-S Medication Solutions
RouteORAL
Drug classDrug class not supplied in source label
Product NDC50090-8045
Label effective date2026-09-09

Official product label reference

Senokot — A-S Medication Solutions

This page contains 13 source sections for STANDARDIZED SENNA, oral route. Label set 0c6e6bdd-9f49-4550-b60a-8f58b7c0f090, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses relieves occasional constipation (irregularity) generally produces a bowel movement in 6–12 hours

Purpose

Purpose Laxative
Dosage and administration — label text
Directions take preferably at bedtime or as directed by a doctor age starting dosage maximum dosage adults and children 12 years of age and over 2 tablets oncea day 4 tablets twicea day children 6 to under12 years 1 tablet once aday 2 tablets twicea day children 2 to under6 years 1/2 tablet oncea day 1 tablet twicea day children under2 years ask a doctor ask a doctor Table text from source: | age | starting dosage | maximum dosage | adults and children 12 years of age and over | 2 tablets oncea day | 4 tablets twicea day | children 6 to under12 years | 1 tablet once aday | 2 tablets twicea day | children 2 to under6 years | 1/2 tablet oncea day | 1 tablet twicea day | children under2 years | ask a doctor | ask a doctor
Warnings
Warnings
Active ingredient
Drug Facts Active ingredient (in each tablet) Sennosides 8.6mg
Do not use
Do not use laxative products for longer than 1 week unless directed by a doctor
Ask a doctor or pharmacist
Aska doctor before use if you have stomach pain nausea vomiting noticed a sudden change in bowel habits that continues overa period of 2 weeks
When to stop use and seek help
Stop use and ask a doctorif you have rectal bleeding or fail to have a bowel movementafter use of a laxative. These may indicate a serious condition.
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children. In case of overdose, get medical help or contact a Poison ControlCenter right away.
Unclassified section
Other Information each tablet contains : calcium 20 mg store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) ©2020 Avrio Health L.P. 305616-0B
Inactive ingredient
Inactive ingredients croscarmellose sodium, dicalciumphosphate, hypromellose, magnesium stearate, maltodextrin, microcrystallinecellulose, mineral oil, polyethylene glycol, talc
Supply and packaging
HOW SUPPLIED Product: 50090-8045 NDC: 50090-8045-0 50 TABLET in a BOTTLE, PLASTIC / 1 in a CARTON

Official sources and product identifiers

Substances listed: SENNOSIDES

RxNorm identifiers: 312935, 404186

Package NDC codes

50090-8045-0

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.