LAXATIVE PILLS MAXIMUM STRENGTH- sennosides tablet, sugar coated 
Walgreen Company

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.

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Walgreens 44-348

Active ingredient (in each tablet)

 Sennosides USP, 25 mg

Purpose

Stimulant laxative

Uses

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

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

Inactive ingredients

acacia, calcium carbonate, carnauba wax, corn starch, dibasic calcium phosphate dihydrate, FD&C blue #1 aluminum lake, iron oxide black, magnesium stearate, maltodextrin*, 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

Well at
Walgreens

WALGREENS PHARMACIST RECOMMENDEDǂ

NDC 0363-0348-08

MAXIMUM STRENGTH
Laxative
Pills
Sennosides USP, 25 mg /
Stimulant Laxative
• Gentle, dependable overnight relief

24
PILLS                Actual Size

Compare to ex•lax® Maximum Strength active ingredientǂǂ

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

ǂWalgreens Pharmacist Survey Study, November 2016.

ǂǂThis product is not manufactured or distributed by GSK group of companies, owner of the registered trademark ex•lax® Maximum Strength.
50844        REV0317C34808

DISTRIBUTED BY: WALGREEN CO.,
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com    ©2017 Walgreen Co.

Walgreens 44-348

Walgreens 44-348

LAXATIVE PILLS  MAXIMUM STRENGTH
sennosides tablet, sugar coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0348
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 25 mg
Inactive Ingredients
Ingredient Name Strength
ACACIA (UNII: 5C5403N26O)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SHELLAC (UNII: 46N107B71O)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Color BLUE Score no score
Shape ROUND Size 10mm
Flavor Imprint Code 44;348
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0363-0348-22 4 in 1 CARTON 01/02/2003
1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2 NDC:0363-0348-08 2 in 1 CARTON 01/02/2003
2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product
3 NDC:0363-0348-52 90 in 1 BOTTLE; Type 0: Not a Combination Product 01/02/2003
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part334 01/02/2003
Labeler - Walgreen Company (008965063)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(0363-0348)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867894 MANUFACTURE(0363-0348)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 967626305 PACK(0363-0348)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867837 PACK(0363-0348)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 868734088 PACK(0363-0348)

Revised: 8/2017
Document Id: 733d239c-9c52-4c20-8bb1-9b1a47f15333
Set id: 3b4b98fe-0067-4d4e-afc1-fd32e8388ef7
Version: 7
Effective Time: 20170818
 
Walgreen Company