EQUALINE STOMACH RELIEF - bismuth subsalicylate tablet 
UNITED NATURAL FOODS, INC. DBA UNFI

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Equaline Stomach Relief Caplets 172

ACTIVE INGREDIENT(in each caplet)

Bismuth subsalicylate 262 mg



PURPOSE

Upset stomach reliever and anti-diarrheal

USE(S)

relieves:


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 behaviour 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 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.

DIRECTIONS

OTHER INFORMATION

INACTIVE INGREDIENTS

calcium carbonate, colloidal silicon dioxide, D&C red 27 lake, magnesium stearate, mannitol, microcrystalline cellulose, polysorbate 80, sodium starch glycolate.

PRINCIPAL DISPLAY PANEL

EQUALINE

Compare to Pepto-Bismol®  active ingredient*

NDC 41163-123-28


Stomach Relief
bismuth subsalicylate 262 mg

anti-diarrheal/upset stomach reliever

relieves:


40 CAPLETS   

172-equ-label.jpg

 




EQUALINE STOMACH RELIEF 
bismuth subsalicylate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-123
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE262 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM CARBONATE (UNII: H0G9379FGK)  
D&C RED NO. 27 (UNII: 2LRS185U6K)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MANNITOL (UNII: 3OWL53L36A)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
Product Characteristics
ColorPINKScoreno score
ShapeCAPSULESize17mm
FlavorImprint Code G;172
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-123-281 in 1 CARTON05/12/2024
140 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drugpart33505/12/2024
Labeler - UNITED NATURAL FOODS, INC. DBA UNFI (943556183)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276MANUFACTURE(41163-123)

Revised: 5/2024
Document Id: a5767e55-97cc-4fe4-a431-668635e205af
Set id: a5767e55-97cc-4fe4-a431-668635e205af
Version: 1
Effective Time: 20240512
 
UNITED NATURAL FOODS, INC. DBA UNFI