Indications and uses
for relief of occasional constipation (irregularity) this product generally produces bowel movement in 6 to 12 hours
Gentle Laxative
- Manufacturer
- L.N.K. International, Inc. | LNK International, Inc.
- Effective date
- 2020-10-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:12:06
Label at a glance#
ProductGentle Laxative WOMENS
Active ingredientBISACODYL
Label structure9 sections
Dosage and administration
do not chew or crush tablets do not take within 1 hour after taking an antacid or milk take with water adults and children 12 years and over: take 1 to 3 tablets in a single dose, once daily children under 12 years: ask a doctor
Storage and handling
TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF) see end flap for expiration date and lot number
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each tablet)
Bisacodyl 5 mg
Purpose
Stimulant laxative
Uses
- for relief of occasional constipation (irregularity)
- this product generally produces bowel movement in 6 to 12 hours
Warnings
Do not use
if you are unable to swallow without chewing.
Ask a doctor before use if you have
- abdominal pain
- nausea
- vomiting
- noticed a sudden change in bowel habits that persists over a period of 2 weeks
When using this product
- abdominal discomfort, faintness, and cramps may occur
- do not use for a period longer than 1 week unless directed by a doctor
Stop use and ask a doctor if
rectal bleeding or failure to have a bowel movement occurs 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 (1-800-222-1222) right away.
Directions
- do not chew or crush tablets
- do not take within 1 hour after taking an antacid or milk
- take with water
- adults and children 12 years and over: take 1 to 3 tablets in a single dose, once daily
- children under 12 years: ask a doctor
Other information
- TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
- store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
- see end flap for expiration date and lot number
Inactive ingredients
anhydrous lactose, carmine, colloidal silicon dioxide, corn starch, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, methacrylic acid, polydextrose, polyethylene glycol, shellac wax, simethicone, sodium bicarbonate, sodium lauryl sulfate, stearic acid, talc, titanium dioxide, triacetin, triethyl citrate
Questions or comments?
1-800-426-9391
Principal display panel
QUALITY
+ PLUS
NDC 50844-676-01
*Compare to active ingredient in Correctol®
WOMEN'S
GENTLE LAXATIVE
Bisacodyl 5 mg •STIMULANT LAXATIVE
Gentle, dependable overnight relief
30 Tablets
ENTERIC COATED 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 Bayer HealthCare LLC, owner of the registered trademark Correctol®.
50844 ORG051567601
Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive
Hauppauge, NY 11788
USA
Products#
Every source-derived product name is available through these pages.
- Gentle Laxative WOMENS
- Bisacodyl
- DEACETYLBISACODYL
- ANHYDROUS LACTOSE
- SILICON DIOXIDE
- STARCH, CORN
- FD&C RED NO. 40
- HYPROMELLOSE, UNSPECIFIED
- MAGNESIUM STEARATE
- METHACRYLIC ACID
- POLYDEXTROSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- SODIUM BICARBONATE
- SODIUM LAURYL SULFATE
- STEARIC ACID
- TALC
- TITANIUM DIOXIDE
- TRIACETIN
- TRIETHYL CITRATE
- SHELLAC
- WATER
- DIMETHICONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50844-676 | 50844-676-01 |
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 |
|---|---|---|---|---|---|---|
| d847780e-67ab-436c-99bd-edabf7e1374d | 81841974-e602-4689-bee5-eb4d0400a53a | 2021-05-07 | Warnings | 81841974-e602-4689-bee5-eb4d0400a53a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.