Senna Syrup
FDA Label NDC 17856-0452

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Atlantic Biologicals Corps for the product Senna Syrup (NDC 17856-0452). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, warnings, directions, indications, purpose, keep out of reach of children, inactive ingredient, label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Each 5ml Contains

Active Ingredient               Purpose

Sennosides 8.8 mg .............Laxative

Warnings

Do not give laxative products to your child for a period longer than 1 week unless directed by a doctor

Directions

Do not exceed recomended dose
Age Starting Dose Maximun Dose
 Adults and Children 2 years and older  2-3 teaspoons once a day preferably at bedtime; increase as needed or as recomended by a doctor 3 teaspoons in the morning and 3 teaspoons at bedtime
 under 12 years of age    ask a doctor ask a doctor

Indications

relieves occasional constipation (irregularity) generally causes bowel movement in 6 to 12 hours

Purpose

Stimulant Laxative

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control center right away.

Inactive Ingredient

Ccoa Distillate Flavor, Methyparaben, Natural Chocolate Flavor, Propylene Glycol, Propylparaben, Purified Water, Sucrose

Label

Label Image (Labelimage)

Label Image (Labelimage)

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