Label: DOCUSATE SODIUM LIQUID- docusate sodium liquid
- NDC Code(s): 17856-1304-1, 17856-1304-2
- Packager: ATLANTIC BIOLOGICALS CORP.
- This is a repackaged label.
- Source NDC Code(s): 0536-1304
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 28, 2025
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENTActive Ingredients (per 5 mL) Docusate Sodium 50 mg
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PURPOSEPurpose - Stool Softener
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INDICATIONS & USAGEUses - Relief of occasional constipation
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WARNINGSWarnings - Do not use when - abdominal pain, nausea, or vomiting are present unless directed by a doctor - for more than one week unless directed by a doctor - Ask a doctore before use if you - are taking ...
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PREGNANCY OR BREAST FEEDINGIf pregnant or breast-feeding, ask a doctor before use
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KEEP OUT OF REACH OF CHILDRENKeep out of reach of children. In case of accidental overdose, seek medical assistance or contact a Poison Control Center right away.
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DOSAGE & ADMINISTRATIONDirections - follow dosing directions below or use as directed by a physician - must be given in a 6 oz to 8 oz glass of milk or fruit juice to prevent throat irritation - may be taken as a single daily ...
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INACTIVE INGREDIENTInactive ingredients: FD&C red #40, flavor, methylparaben, poloxamer, polyethylene glycol, propylene glycol, propylparaben, sodium benzoate, sodium citrate, sucralose - DISTRIBUTED BY - ATLANTIC ...
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QUESTIONSQuestions or comments? 1-800-509-7592
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INGREDIENTS AND APPEARANCEProduct Information