Indications and uses
relieves occasional constipation (irregularity) generally produces bowel movement in 6 to 12 hours
Laxative
- Manufacturer
- Topco Associates, LLC | LNK International, Inc.
- Effective date
- 2023-10-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:24:15
Label at a glance#
ProductLaxative Maximum Strength
Active ingredientSENNOSIDES
Label structure9 sections
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 and over 2 tablets once or twice daily children 6 to under 12 years 1 tablet once or twice daily children under 6 years ask a doctor
Storage and handling
each tablet contains: calcium 40 mg, magnesium 5 mg TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) see end flap for expiration date and lot number
Contacts and useful links#
Websitewww.topcarebrand.com
www.topcarebrand.com
www.topcarebrand.comLabel contents#
Full prescribing information#
Active ingredient (in each tablet)
Sennosides USP, 25 mg
Purpose
Stimulant laxative
Uses
- relieves occasional constipation (irregularity)
- generally produces bowel movement in 6 to 12 hours
Warnings
Do not use
laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor.
Ask a doctor before use if you have
noticed a sudden change in bowel habits that persists over a period of 2 weeks.
Ask a doctor or pharmacist before use if you 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,
do not use for a period longer than 1 week.
Stop use and ask a doctor if
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,
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.
Directions
- swallow tablet(s) with a glass of water
- swallow tablet(s) whole; do not crush, break, or chew
| adults and children 12 years and over | 2 tablets once or twice daily |
| children 6 to under 12 years | 1 tablet once or twice daily |
| children under 6 years | ask a doctor |
Other information
- each tablet contains: calcium 40 mg, magnesium 5 mg
- TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
- store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
- see end flap for expiration date and lot number
Inactive ingredients
acacia, calcium carbonate, carnauba wax, corn starch, dibasic calcium phosphate dihydrate, FD&C blue #1 aluminum lake, iron oxide black, magnesium stearate, methylparaben, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, propylene glycol, propylparaben, shellac glaze, silicon dioxide, sodium benzoate, sodium lauryl sulfate, sucrose, talc, titanium dioxide
Questions or comments?
1-888-423-0139
Principal Display Panel
+TopCare®
health
NDC 36800-305-08
COMPARE TO EX•LAX®
MAXIMUM STRENGTH
ACTIVE INGREDIENT†
MAXIMUM STRENGTH
Laxative
SENNOSIDES USP, 25 mg • STIMULANT LAXATIVE
• Senna Ingredient
• Gentle, Dependable Constipation Relief
24 COATED TABLETS
actual
size
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
†This product is not manufactured or distributed
by GSK Consumer Healthcare S.A., owner of the
registered trademark ex•lax® Maximum Strength.
✓QUALITY GUARANTEED
50844
ORG041934808
DISTRIBUTED BY
TOPCO ASSOCIATES LLC
ELK GROVE VILLAGE, IL 60007
©TOPCO LNKA0221
QUESTIONS? 1-888-423-0139
topcare@topco.com
www.topcarebrand.com
Products#
Every source-derived product name is available through these pages.
- Laxative Maximum Strength
- Sennosides
- ACACIA
- CALCIUM CARBONATE
- CARNAUBA WAX
- STARCH, CORN
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE
- FD&C BLUE NO. 1 ALUMINUM LAKE
- FERROSOFERRIC OXIDE
- MAGNESIUM STEARATE
- METHYLPARABEN
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYVINYL ALCOHOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- PROPYLENE GLYCOL
- PROPYLPARABEN
- SHELLAC
- SILICON DIOXIDE
- SODIUM BENZOATE
- SODIUM LAURYL SULFATE
- SUCROSE
- TALC
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 36800-305 | 36800-305-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ce11001d-fbd3-4cd9-aabf-00bae620b2c5 | 60ea0f82-d24d-4390-aabd-b56a74df42ac | 2023-10-11 | Warnings | ce11001d-fbd3-4cd9-aabf-00bae620b2c5 60ea0f82-d24d-4390-aabd-b56a74df42ac |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.