Indications and uses
relieves occasional constipation (irregularity) generally produces bowel movement un 6 to 12 hours
Laxative Pills
- Manufacturer
- QUALITY CHOICE (Chain Drug Marketing Association)
- Effective date
- 2019-11-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:01:59
Label at a glance#
ProductLaxative Pills Maximum Strength
Active ingredientSENNOSIDES
Label structure10 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 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 50 mg very low sodium store between 20-25ºC (68-77ºF)
Contacts and useful links#
Websitewww.qualitychoice.com
www.qualitychoice.com
www.qualitychoice.comLabel contents#
Full prescribing information#
Active ingredient (in each tablet)
Sennosides 25 mg
Purpose
Stimulant laxative
Uses
- relieves occasional constipation (irregularity)
- generally produces bowel movement un 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 a prescription 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 movemenr 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 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 |
Other information
- each tablet contains: calcium 50 mg
- very low sodium
- store between 20-25ºC (68-77ºF)
Inactive ingredients
acacia, ammonium hydroxide*, calcium carbonate*, calcium phosphate dihydrate*, calcium sulfate anhydrous*, carnauba wax, corn starch*, croscarmellose sodium, dicalcium phosphate*, FD&C blue #1, hypromellose*, iron oxide*, iron oxide black, iron oxide yellow*, isopropyl alcohol*, kaolin*, magnesium stearate, maltodextrin, microcrystalline cellulose, mineral oil*, n-butyl alcohol*, polyethylene glycol, polyvinyl alcohol*, povidone*, propylene glycol*, shellac*, silicon dioxide, sodium lauryl sulfate*, stearic acid, sucrose, talc, titanium dioxide, white wax*
*contains one or more of these ingredients
Questions or Comments?
Call 1-248-449-9300 Monday-Friday 9AM-5PM EST
Principal Display Panel
†Compare to the active ingredient in ex-lax® MAXIMUM STRENGTH
Maximum Strength
Laxative
Stimulant Laxative
Sennosides 25 mg
gentle, dependable overnight relief
TABLETS
TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
†This product is not manufactured or distributed by Novartis, owner of the registered trademark Ex-Lax®
Distributed by C.D.M.A., Inc.©
43157 W. Nine Mile
Novi, MI 48376-0995
Product Label
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63868-086-24 | EA - Each | 63868-086 | 9864a314-030f-430b-ade2-37a50ba1381e | 1 | 2019-02-13 |
Products#
Every source-derived product name is available through these pages.
- Laxative Pills Maximum Strength
- Sennosides
- ACACIA
- AMMONIA
- CALCIUM CARBONATE
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE
- CALCIUM SULFATE ANHYDROUS
- CARNAUBA WAX
- STARCH, CORN
- CROSCARMELLOSE SODIUM
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE
- FD&C BLUE NO. 1
- HYPROMELLOSES
- FERRIC OXIDE RED
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- ISOPROPYL ALCOHOL
- KAOLIN
- MAGNESIUM STEARATE
- MALTODEXTRIN
- CELLULOSE, MICROCRYSTALLINE
- MINERAL OIL
- BUTYL ALCOHOL
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYVINYL ALCOHOL, UNSPECIFIED
- POVIDONE
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- STEARIC ACID
- SUCROSE
- TALC
- TITANIUM DIOXIDE
- WHITE WAX
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63868-086 | 63868-086-24 |
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 |
|---|---|---|---|---|---|---|
| 4e8dbf4d-856e-45d7-b993-bcc4939fc2de | 5326f545-748f-44c5-bbb7-e8b2c404bf60 | 2019-11-11 | Warnings | 4e8dbf4d-856e-45d7-b993-bcc4939fc2de 5326f545-748f-44c5-bbb7-e8b2c404bf60 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.