Otc - Active Ingredient
psyllium husk powder, sennae fructus powder
Laxatives Rubilax Granule
FDA Label NDC 72988-0010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lydia Co., Ltd. for the product Laxatives Rubilax (NDC 72988-0010). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
lactose monohydrate, acacia, corn starch, carboxymethylcellulose calcium, l-menthol
Otc - Purpose
constipation
relieving the following symptoms of constipation: loss of appetite, abdominal distension, intestinal fermentation, hemorrhoids
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
adults take intake does of 3.5g twice a day morning and evening on an empty stomach, however, taking the minimum amount of the first time and watching the shape and condition of the stomach gradually increases or decreases
Warnings
do not administer to the following patients,
the product contains lactose, patients with rare hereditary problems of galactose intolerance, the lapp deficiency or glucose-galactose malabsorption should not take this medicine
Dosage & Administration
for oral use only
Package Label.Principal Display Panel
Label (Label)
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