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Mineral oil - Medication Information

Product NDC Code 17856-1110
Drug Name

Mineral oil

Type Generic
Active Ingredients
Mineral oil 999 mg/ml
Route ORAL
Dosage Form LIQUID
RxCUI drug identifier 705909
Application Number M
Labeler Name ATLANTIC BIOLOGICALS CORP.
Packages
Package NDC Code Description
17856-1110-1 50 cup, unit-dose in 1 box, unit-dose (17856-1110-1) / 30 ml in 1 cup, unit-dose (17856-1110-2)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Mineral oil 99.9%

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 do not take with meals take only at bedtime may be taken as a single daily dose or in divided doses adults and children 12 years of age and over - 1 to 3 Tablespoons (15 to 45 mL) maximum 3 Tablespoons (45 mL) in 24 hours children 6 to under 12 years of age - 1 to 3 teaspoons (5 to 15 mL) maximum 3 teaspoons (15 mL) in 24 hours children under 6 years of age - do not use, consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients mixed tocopherols (added as a stabilizer)

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.
Use for relief of occasional constipation (irregularity). Generally produces bowel movement in 6 to 8 hours.

Purpose

Information about the drug product’s indications for use.
Purpose Lubricant laxative

Spl product data elements

Usually a list of ingredients in a drug product.
Mineral Oil Mineral Oil MINERAL OIL MINERAL OIL TOCOPHEROL

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.
Principal Display Panel NDC 17856-1110-01 image description

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.
Distributed by: McKesson Corp. Via Strategic Services LLC. Memphis, TN 38141 Money Back Guarantee www.fosterandthrive.com (c) 2023 McKesson Corporaation You may report serious side effects to 833-358-6431 Monday to Friday 9:00am to 7:00pm EST

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have abdominal pain, nausea, or vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you are presently taking a stool softener laxative taking any other drug. Take this product 2 or more hours before or after other drugs. Laxatives may affect how other drugs work.

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. In case of overdose, get medical help or contact a Poison Control Center right away.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use. These could be signs of a serious condition.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not take with meals. Take only at bedtime.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If breast-feeding, ask a health professional before use.

Storage and handling

Information about safe storage and handling of the drug product.
Other Information keep tightly closed. Protect from sunlight.

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 have difficulty swallowing in children under 6 years of age if you are pregnant for a period longer than 1 week if you are bedridden or aged

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