CARTERS LITTLE PILLS  SODIUM-FREE- bisacodyl tablet, delayed release 
Church & Dwight Co., Inc.

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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Active ingredient (in each tablet)

Bisacodyl USP, 5 mg


Purpose

Stimulant laxative

Uses

Warnings

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

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

Follow dosage below or use a directed by a doctor

adults and children 12 years of age and over                                    1 to 3 tablets (usually 2) in a single daily dose

children 6 to under 12 years of age                                                  1 tablet in a single daily dose

children under 6 years of age                                                           consult a doctor

Other information

Questions or Comments:  1-800-926-5222 M-F from 9-5 ET

Inactive ingredients

Croscarmellose Sodium, Hydroxypropyl Methylcellulose, Lactose, Magnesium Stearate, Methacrylic Acid Copolymer, Microcrystalline Cellulose, Talc, Triacetin, Triethyl Citrate, Zea mays (Corn) Starch


Principal Display

Overnight Relief Guaranteed

CARTERS

LITTLE

PILLS

Carter's

BISACODYL DELAYED-RELEASED TABLETS

STIMULANT LAXATIVE

Sodium-Free

ENTERIC COATED 25 TABLETS

Carton image Carton image

CARTERS LITTLE PILLS   SODIUM-FREE
bisacodyl tablet, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-906
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL5 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)  
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize6mm
FlavorImprint Code C;5
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-906-251 in 1 CARTON06/01/201111/14/2018
125 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:10237-906-753 in 1 CARTON06/01/201111/14/2018
225 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33406/01/2011
Labeler - Church & Dwight Co., Inc. (001211952)
Establishment
NameAddressID/FEIBusiness Operations
Church & Dwight Canada Corp.253933600manufacture(10237-906)

Revised: 1/2023
Document Id: f1b4de1e-8f1c-2892-e053-2a95a90a10e9
Set id: 4ee15f4b-070e-4f6a-a3ff-dbb5136f8db6
Version: 5
Effective Time: 20230107
 
Church & Dwight Co., Inc.