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Laxative Maximum Strength by L.N.K. International, Inc.

Medically reviewed on June 15, 2017

Dosage form: tablet
Ingredients: SENNOSIDES 25mg
Labeler: L.N.K. International, Inc.
NDC Code: 50844-948

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Sound Body 44-348

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 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 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 (1-800-222-1222) 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 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 40 mg, mahnesium 5 mg
  • 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

acacia, calcium carbonate, carnauba wax, corn starch, dibasic calcium phosphate dihydrate, FD&C blue #1 aluminum lake, iron oxide black, magnesium stearate, methylparaben, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, propylene glycol, propylparaben, shellac glaze, silicon dioxide, sodium benzoate, sodium lauryl sulfate, sucrose, talc, titanium dioxide

Questions or comments?

1-800-426-9391 

Principal Display Panel

SOUND
BODY

*Compare to the
active ingredient
in exlax®
Maximum Strength

MAXIMUM STRENGTH

Laxative

Sennosides USP, 25 mg
Stimulant Laxative

Gentle, Dependable Overnight Relief

24 Tablets

Actual Size 

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING

*This product is not manufactured or distributed by GSK group of companies, owner of the registered trademark ex•lax® Maximum Strength.
50844       REV0317B34808

Distributed by
LNK INTERNATIONAL, INC.,
60 Arkay Drive,
Hauppauge, NY 11788 USA
V#733000
ITEM#022734808BLBX

Sound Body 44-348

LAXATIVE  MAXIMUM STRENGTH
sennosides tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50844-948
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SENNOSIDES (SENNOSIDES) SENNOSIDES25 mg
Inactive Ingredients
Ingredient NameStrength
ACACIA 
CALCIUM CARBONATE 
CARNAUBA WAX 
STARCH, CORN 
FD&C BLUE NO. 1 
FERROSOFERRIC OXIDE 
MAGNESIUM STEARATE 
METHYLPARABEN 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOLS 
POVIDONE 
PROPYLENE GLYCOL 
PROPYLPARABEN 
SHELLAC 
SODIUM BENZOATE 
SODIUM LAURYL SULFATE 
SUCROSE 
TALC 
TITANIUM DIOXIDE 
SILICON DIOXIDE 
Product Characteristics
ColorBLUEScoreno score
ShapeROUNDSize10mm
FlavorImprint Code44;348
Contains    
Packaging
#Item CodePackage Description
1NDC:50844-948-082 BLISTER PACK in 1 CARTON
112 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart33401/02/2003
Labeler - L.N.K. International, Inc. (038154464)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(50844-948)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(50844-948)

 
L.N.K. International, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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