Laxative

Manufacturer
EQUALINE (SuperValu)
Effective date
2022-12-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:45:28

Label at a glance#

ProductLaxative Maximum Strength
Active ingredientSENNOSIDES
Label structure10 sections

Indications and uses

relieves occasional constipation (irregularity) generally produces bowel movement in 6 to 12 hours

Dosage and administration

swallow tablet(s) with a glass of water swallow tablet(s) whole, do not crush, break, or chew adults and children 12 years of age and older take 2 tablets once or twice daily  children 6 to under 12 years of age take 1 tablet once or twice daily children under 6 years of age  ask a doctor

Storage and handling

each tablet contains : calcium 40 mg very low sodium store between 20-25ºC (68-77ºF)

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Sennosides USP, 25 mg

Purpose

OTC - PURPOSE SECTION

Stimulant laxative

Uses

INDICATIONS & USAGE SECTION

  • relieves occasional constipation (irregularity)
  • generally produces bowel movement in 6 to 12 hours

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor. 

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • noticed a sudden change in bowel habits that persists over a period of 2 weeks

Ask a doctor or pharmacist before use if you

OTC - ASK DOCTOR/PHARMACIST SECTION

  • are taking any other drug. Laxatives may affect how other drugs work. Take this product 2 or more hours before or after other drugs.

When using this product

OTC - WHEN USING SECTION

  • do not use for a period longer than 1 week

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rectal bleeding or failure to have a bowel movement occur after use of a laxative

These may be signs of a serious condition.

If pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • swallow tablet(s) with a glass of water
  • swallow tablet(s) whole, do not crush, break, or chew
adults and children 12 years of age and oldertake 2 tablets once or twice daily 
children 6 to under 12 years of agetake 1 tablet once or twice daily
children under 6 years of age ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • each tablet contains: calcium 40 mg
  • very low sodium
  • store between 20-25ºC (68-77ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acacia, calcium phosphate dihydrate, calcium sulfate anhydrous*, carnauba wax, corn starch*, croscarmellose sodium, FD&C blue #1 aluminum lake,  iron oxide*, iron oxide black, iron oxide yellow*, kaolin, magnesium stearate, maltodextrin, microcrystalline cellulose,  polyethylene glycol, povidone*, shellac, silicon dioxide*, stearic acid*, sugar, talc, titanium dioxide

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-877-932-7948 

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

compare to ex-lax® Maximum Strength active ingredient†

maximum strength

Laxative

Sennosides USP, 25 mg

(stimulant laxative)

gentle, dependable overnight relief

tablets

†This product is not manufactured or distributed by GlaxoSmithKline plc, distributor of ex-lax®

TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

DISTRIBUTED BY SUPERVALU INC., EDEN PRAIRE, MN 55344 USA

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQUALINE Maximum Strength Laxative
EQUALINE Maximum Strength Laxative

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41163-81541163-815-24, 41163-815-48

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
78abaf4d-038f-4e7f-8eee-4acf676fc07c4a9376d7-c396-4753-950d-dd9bcae673f82024-06-13WarningsExact identifier
spl set id: 4a9376d7-c396-4753-950d-dd9bcae673f8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.