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Safety Data Sheet SDS created:2920221 Identification of substance and manufacturer Axon catalogue ID 3640 Product name Loperamide hydrochloride IUPAC name 4(4(4Chlorophenyl)4hydroxypiperidin1yl)N,Ndimethyl2,2diphenylbutanamide
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Begin by gathering all necessary information about the patient and their medical history.
02
Ensure you have the correct dosage information as prescribed by the healthcare provider.
03
Write the patient's name clearly on the label.
04
Include the dosage strength of the loperamide hydrochloride capsule on the label.
05
Specify the directions for use, such as 'Take one capsule after each loose stool, not to exceed 8 capsules in 24 hours.'
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Provide any necessary cautionary statements, such as advises against use in certain medical conditions.
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Include the expiration date and lot number for tracking purposes.
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Double-check all information for accuracy before finalizing the label.

Who needs label loperamide hydrochloride capsule?

01
Individuals experiencing acute diarrhea or those recommended loperamide by their healthcare provider.
02
Patients who require a medication to manage bowel movements due to conditions like Irritable Bowel Syndrome (IBS).
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Travelers who may be at risk of developing diarrhea while away from home.
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People recovering from gastrointestinal surgery may also need this medication.
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Loperamide hydrochloride capsule is a medication used to manage diarrhea. It works by slowing down the movement in the gut, which decreases the number of bowel movements and makes the stool less watery.
Manufacturers of loperamide hydrochloride capsules are required to file the label with regulatory authorities to ensure compliance with safety and efficacy standards.
Filling out the label involves providing detailed information about the drug, including the active ingredients, dosage instructions, indications, contraindications, side effects, storage information, and manufacturer details.
The purpose of the label is to inform healthcare professionals and patients about the proper use of loperamide hydrochloride capsules, including dosage, usage, potential side effects, and warnings.
The label must report information such as the drug's active ingredients, dosage instructions, indications for use, contraindications, warnings, side effects, storage conditions, and manufacturer contact information.
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