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

Medically reviewed on Apr 21, 2018

Dosage form: tablet, sugar coated
Ingredients: SENNOSIDES 25mg
Labeler: L.N.K. International, Inc.
NDC Code: 50844-348

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.

Quality Plus 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 of age 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, magnesium 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 to 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

QUALITY
✚PLUS

NDC 50844-348-02

*Compare to the active ingredient in ex•lax® Maximum Strength

Maximum Strength
Laxative
Sennosides USP, 25 mg
Stimulant Laxative
Gentle, Dependable
Overnight relief

12 Coated Tablets
ACTUAL SIZE

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

Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive
Hauppauge, NY 11788
USA

†This product is not manufactured  or distributed by GSK group of companies, owner of the registered trademark ex•lax® Maximum Strength.
50844    REV0317B34802

Quality Plus 44-348


LAXATIVE  MAXIMUM STRENGTH
sennosides tablet, sugar coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50844-348
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 
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS 
FD&C BLUE NO. 1 
MAGNESIUM STEARATE 
METHYLPARABEN 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOL, UNSPECIFIED 
PROPYLENE GLYCOL 
PROPYLPARABEN 
SHELLAC 
SODIUM BENZOATE 
SODIUM LAURYL SULFATE 
SUCROSE 
TALC 
TITANIUM DIOXIDE 
STARCH, CORN 
FERROSOFERRIC OXIDE 
SILICON DIOXIDE 
Product Characteristics
ColorBLUEScoreno score
ShapeROUNDSize10mm
FlavorImprint Code44;348
Contains    
Packaging
#Item CodePackage Description
1NDC:50844-348-021 BLISTER PACK in 1 CARTON
112 TABLET, SUGAR COATED 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(50844-348)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(50844-348)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(50844-348)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088PACK(50844-348)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(50844-348)

 
L.N.K. International, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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