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OTC products · Product label record

Kroger Stool Softener Fruit Punch drug information

DOCUSATE SODIUM
KROGER COMPANY · ORAL

Product NDC: 41226-714

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameDOCUSATE SODIUM
Labeler / manufacturerKROGER COMPANY
RouteORAL
Drug classDrug class not supplied in source label
Product NDC41226-714
Label effective date2026-09-02

Official product label reference

Kroger Stool Softener Fruit Punch — KROGER COMPANY

This page contains 11 source sections for DOCUSATE SODIUM, oral route. Label set b86f8f3d-594e-466c-854a-b8bff9f7a0b8, version 5.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses • relieves occasional constipation (irregularity) • generally produces bowel movement in 12-72 hours

Purpose

Purpose Stool Softener
Dosage and administration — label text
Directions • follow dosing directions below or take as directed by doctor • must be given in a 6 to 8 oz glass of milk or fruit juice to prevent throat irritation • may be taken as a single daily dose or in divided doses • take maximum dose daily until first bowel movement, dosage should then be reduced according to individual response. • do not exceed recommended dose • shake well before using Age Dose Adults and children 12 years and over 5 mL-30 mL Children 2 to under 12 years 5 mL-15 mL Table text from source: | Age | Dose | Adults and children 12 years and over | 5 mL-30 mL | Children 2 to under 12 years | 5 mL-15 mL
Warnings
Warnings Do not use • laxative products for longer than 1 week unless directed by a doctor Ask a doctor before use if you have • stomach pain • nausea • vomiting • noticed a sudden change in bowel habits that continues over a period of 2 weeks Stop use and ask a doctor if rectal bleeding of fail to have a bowel movement after use of laxative. These may indicate a serious condition.
Active ingredient
Active ingredient (in each 5 mL) Docusate Sodium 50 mg
Pregnancy or breast feeding
If pregnant or breast feeding , ask a health professional before use.
Child safety
Keep out of reach of children . In case of overdose, get medical help or contact a poison control Center right away at 1-800-222-1222.
Other safety information
Other information • each 5 mL contains: sodium 6 mg • low sodium • store at room temperature • protect from excessive heat • keep tightly closed • protect from light SAFETY SEALED: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING
Inactive ingredient
Inactive ingredients Benzyl alcohol, citric acid, flavor, polyethylene glycol, povidone, propylene glycol, purified water, sodium citrate, sorbitol, sucralose, xanthan gum.
Questions
Questions or comments? 1-866-467-2748
Package label principal display panel
Table text from source: | IMPORTANT: Keep this carton for future reference on full labeling.

Official sources and product identifiers

Substances listed: DOCUSATE SODIUM

RxNorm identifiers: 1248119

Package NDC codes

41226-714-08

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.