Indications and uses
relieves occasional constipation (irregularity) generally produces bowel movement in 6 to 12 hours
HEB 44-773
- Manufacturer
- H E B | LNK International, Inc.
- Effective date
- 2026-10-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- daily-update
- Hydrated at
- 2026-10-17 02:02:48
Label at a glance#
ProductLaxative Maximum Strength
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
Compare to ex•lax® Maximum Strength active ingredient*
NDC 37808-779-08
H - E - B ®
Maximum Strength
Laxative Pills
Sennosides USP, 25 mg
Stimulant Laxative
Gentle, Dependable Constipation Relief
actual size
24 TABLETS
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0197870108735 | GTIN-13: 0197870108735 EAN-13: 0197870108735 GTIN-12: 197870108735 UPC-A: 197870108735 GTIN storage (14 digits): 00197870108735 | heb-44-773-1.jpg |
Products#
Every source-derived product name is available through these pages.
- Laxative Maximum Strength
- 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 |
|---|---|
| 37808-779 | 37808-779-52, 37808-779-08 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.