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| Product NDC Code | 55154-9630 | ||||
|---|---|---|---|---|---|
| Drug Name | Docu liquid |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | ORAL | ||||
| Dosage Form | LIQUID | ||||
| RxCUI drug identifier | 1248119 | ||||
| Application Number | M007 | ||||
| Labeler Name | Cardinal Health 107, LLC | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient Docusate Sodium 50 mg
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions • may be taken once daily or in divided doses • give dose in 1/2 glass of milk, fruit juice or infant formula to mask bitter taste and prevent throat irritation adults and children over 12 1 to 7 teaspoons children 2 to under 12 1 to 3 teaspoons children under 2 ask a doctor
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients D&C Red #33, methylparaben, natural & artificial vanilla flavor, poloxamer 181, polyethylene glycol, propylene glycol, propylparaben, purified water, sodium benzoate. Sodium citrate may be used to adjust pH.
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses • relieves occasional constipation • generally produces bowel movement in 12-72
Purpose
Information about the drug product’s indications for use.Purpose Stool Softener Laxative
Spl product data elements
Usually a list of ingredients in a drug product.Docu Liquid Docusate Sodium DOCUSATE SODIUM DOCUSATE D&C RED NO. 33 METHYLPARABEN POLYETHYLENE GLYCOL 400 PROPYLENE GLYCOL PROPYLPARABEN SODIUM BENZOATE SODIUM CITRATE, UNSPECIFIED FORM WATER POLOXAMER 181 natural and artificial flavor
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.Package/Label Principal Display Panel DOCU LIQUID (DOCUSATE SODIUM) 100 mg/ 10 mL STOOL SOFTENER LAXATIVE 5 Cups bag label
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Other information • each teaspoon contains: sodium 5 mg • shake well before using • store at controlled room temperature 15° - 30°C (59° - 86°F) • dispense contents with a child resistant closure in a tight, light resistant container as defined in the USP • store in an upright position
Questions or comments? • Call 1-800-932-5676 Mon - Thurs. 9:00 am - 4:30 pm EST, Fri. 9:00 am - 2:30 pm EST. Serious side effects associated with use of this product may be reported to this number. Distributed By: Cardinal Health Dublin, OH 43017 L57365410522
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.Do Not Use • if you are presently taking mineral oil • when abdominal pain, nausea, or vomiting are present • for longer than one week
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep Out of Reach of Children
Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings Do Not Use • if you are presently taking mineral oil • when abdominal pain, nausea, or vomiting are present • for longer than one week Ask a doctor before use if you have noticed a sudden change in bowel habits that lasts over two weeks. Ask a doctor or pharmacist before use if you are taking any other drug. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work. Stop use and ask a doctor if • you have rectal bleeding • you fail to have a bowel movement after use of this product 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.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API