5 SYMPTOM DIGESTIVE RELIEF- bismuth subsalicylate tablet, chewable 
TARGET CORPORATION

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Target Bismuth Subsalicylate Chewable Tablets 262 mg

Drug Facts

Active ingredient (in each tablet)

Bismuth subsalicylate 262 mg

Purpose

Upset stomach reliever and antidiarrheal

Uses relieves

-travelers' diarrhea
-diarrhea
-upset stomach due to overindulgence in food and drink, including:

Warnings

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Allergy alert: Contains salicylate. Do not take if you are

Do not use if you have

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are taking any drug for

When using this product a temporary, but harmless, darkening of the stool and/or tongue may occur

Stop use and ask a doctor if

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 (1-800-222-1222).

Directions

-2 tablets (1 dose) every ½ hour or 4 tablets (2 doses) every hour as needed for diarrhea

-2 tablets (1 dose) every ½ hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea)

Other information

Inactive ingredients calcium carbonate, D&C red #27 lake, flavor, magnesium stearate, mannitol, povidone, saccharin sodium, talc

Questions or comments? Call 1-800-910-6874

bismuth-48ct-ifc

5 SYMPTOM DIGESTIVE RELIEF 
bismuth subsalicylate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-723
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ, BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE262 mg
Inactive Ingredients
Ingredient NameStrength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
TALC (UNII: 7SEV7J4R1U)  
MANNITOL (UNII: 3OWL53L36A)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Product Characteristics
Colorpink (Light pink to pink) Scoreno score
ShapeROUNDSize15mm
FlavorImprint Code 118
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-723-488 in 1 CARTON06/15/2024
16 in 1 CELLO PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00806/15/2024
Labeler - TARGET CORPORATION (006961700)
Registrant - TIME CAP LABORATORIES, INC. (037052099)
Establishment
NameAddressID/FEIBusiness Operations
MARKSANS PHARMA LIMITED925822975manufacture(11673-723)

Revised: 5/2024
Document Id: 1945a7a8-d9f2-7ad0-e063-6394a90a7b5e
Set id: 07a932fb-38eb-4b35-e063-6394a90ad61f
Version: 2
Effective Time: 20240525
 
TARGET CORPORATION