FDA Label for Sennosides
View Indications, Usage & Precautions
Sennosides Product Label
The following document was submitted to the FDA by the labeler of this product H E B. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
(in each softgel)
Sennosides 17.2 mg
Purpose
Laxative
Uses
■ relieves occasional constipation (irregularity)
■ generally produces a bowel movement within 6-12 hours
Do Not Use
■ laxative products for longer than 1 week unless directed by a doctor
Ask A Doctor Before Use If You Have
■ stomach pain
■ nausea
■ vomiting
■ noticed a sudden change in bowel habits that continues over a period of 2 weeks
Stop Use And Consult A Doctor If
you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate a serious condition.
If Pregnant Or Breast-Feeding
ask a health professional before use
Keep Out Of Reach Of Children.
In case of overdose, get medical help or contact a Poison Control Center right away
Directions
■ 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
Other Information
■ store below 30°C and protect from light and moisture
Inactive Ingredients
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.
Questions Or Comments?
call 1-877-770-3183: weekdays 9:00 AM to 4:30 PM EST.
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