Indications and uses
relieves occasional constipation (irregularity) generally produces bowel movement in 6 to 12 hours
Laxative
- Manufacturer
- L.N.K. International, Inc. | LNK International, Inc.
- Effective date
- 2024-07-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 00:15:52
Label at a glance#
ProductLaxative
Active ingredientSENNOSIDES
Label structure9 sections
Dosage and administration
do not take more than directed 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 35 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#
Label 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
- do not take more than directed
- 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 35 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
corn starch, dibasic calcium phosphate dihydrate, FD&C blue #1 aluminum lake, hypromellose, magnesium stearate, medium chain triglycerides, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, sodium lauryl sulfate, sucrose, talc, titanium dioxide
Questions or comments?
1-800-426-9391
Principal display panel
SOUNDBODY™
*Compare to the
active ingredient
in ex•lax®
Maximum Strength
NDC 50844-073-08
MAXIMUM STRENGTH
Laxative
Sennosides USP, 25 mg
Stimulant Laxative
Gentle, Dependable Constipation Relief
24 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 SARL,
owner of the registered trademark ex•lax®
Maximum Strength.
50844 ORG082177308
Manufactured for
Big Lots Stores, Inc.
by LNK INTERNATIONAL, INC.
60 Arkay Drive, Hauppauge, NY
11788 USA
V#733000
ITEM#022777308BLBX
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Laxative
- Sennosides
- STARCH, CORN
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE
- FD&C BLUE NO. 1 ALUMINUM LAKE
- HYPROMELLOSE, UNSPECIFIED
- MAGNESIUM STEARATE
- MEDIUM-CHAIN TRIGLYCERIDES
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYVINYL ALCOHOL, UNSPECIFIED
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- SUCROSE
- TALC
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50844-073 | 50844-073-08 |
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 |
|---|---|---|---|---|---|---|
| 963664df-b12f-4f19-a2ec-45160cfc5a7c | 5f32a3f8-859d-4dca-aa25-3636eefd7cbc | 2024-07-23 | Warnings | 963664df-b12f-4f19-a2ec-45160cfc5a7c 5f32a3f8-859d-4dca-aa25-3636eefd7cbc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.