Active Ingredient
(in each softgel)
Sennosides 17.2 mg
The following Structured Product Label (SPL) was submitted to the FDA by H E B for the product Sennosides (NDC 37808-712). 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, purpose, uses, do not use, ask a doctor before use if you have, stop use and consult a doctor if, if pregnant or breast-feeding, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
(in each softgel)
Sennosides 17.2 mg
Laxative
■ relieves occasional constipation (irregularity)
■ generally produces a bowel movement within 6-12 hours
■ laxative products for longer than 1 week unless directed by a doctor
■ stomach pain
■ nausea
■ vomiting
■ noticed a sudden change in bowel habits that continues over a period of 2 weeks
you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate a serious condition.
ask a health professional before use
In case of overdose, get medical help or contact a Poison Control Center right away
■ take preferably at bedtime or as directed by a doctor.
adults and children 12 years and over
■ 1 capsule once a day. Maximum 2 capsules twice a day.
children 6 to under 12 years
■ maximum 1 capsule twice a day
children under 6 years
■ ask a doctor
■ store below 30°C and protect from light and moisture
FD&C blue no.1, FD&C blue no.2, FD&C red no. 40, FD&C yellow no.6, fumaric acid, gelatin, glycerol, lecithin, liquid sorbitol, methyl hydroxy benzoate, purified water, refined soya oil, titanium dioxide, yellow bees wax.
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