Active Ingredient (In Each Tablet)
Sennosides USP, 25 mg
The following Structured Product Label (SPL) was submitted to the FDA by Family Dollar Services Inc for the product Laxative (NDC 55319-773). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, when using this product,, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Sennosides USP, 25 mg
Stimulant laxative
laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor
noticed a sudden change in bowel habits that persists over a period of 2 weeks.
taking any other drug. Laxatives may affect how other drugs work. Take this product 2 or more hours before or after other drugs.
do not use for a period longer than 1 week.
rectal bleeding or failure to have a bowel movement occur after use of a laxative. These may be signs of a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
| 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 |
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
1-800-426-9391
FAMILY
Wellness™
*COMPARE TO THE ACTIVE
INGREDIENT IN ex•lax®
MAXIMUM STRENGTH
MAXIMUM STRENGTH
LAXATIVE
Sennosides USP, 25 mg
Stimulant Laxative
Gentle, Dependable Constipation Relief
24 TABLETS
OVERNIGHT
RELIEF
ACTUAL SIZE
NDC 55319-773-08
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
DISTRIBUTED BY:
MIDWOOD BRANDS LLC,
500 VOLVO PKWY
CHESAPEAKE, VA 23320 USA
NOT 100% SATISFIED?
Return within 30 days to the
store of purchase for a refund
(with receipt) or exchange.
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