QC STOMACH RELIEF REGULAR STRENGTH- bismuth subsalicylate liquid 
QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)

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Quality Choice Max Strength Bismuth Subsalicylate 525mg

Active ingredient (in each 15 mL)

Bismuth subsalicylate 525 mg

Purpose

Upset stomach reliever/Antidiarrheal

Uses

relieves

travelers' diarrhea
diarrhea
upset stomach due to overindulgence in food and drink, including:
heartburn
indigestion
upset stomach
nausea
gas
belching

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

allergic to salicylates (including aspirin)
taking other salicylate products

Do not use

if you have

an ulcer
a bleeding problem
bloody or black stool

Ask a doctor before use if you have

fever
mucus in the stool

Ask a doctor or pharmacist before use if you are

taking any drug for

anticoagulation (thinning the blood)
diabetes
gout
arthritis

When using this product

a temporary, but harmless, darkening of the stool and/or tongue may occur.

Stop use and ask a doctor if

symptoms get worse
ringing in the ears or loss of hearing occurs
diarrhea lasts more than 2 days

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

shake well before use
For accurate dosing, use dose cup
adults and children 12 years and over:
1 dose (2 tbsp. or 30 ml) every 1 hour as needed
do not exceed 4 doses (8tbsp or 120 mL) in 24 hours
use until diarrhea stops but not more than 2 days
children under 12 years: ask a doctor
drink plenty of clear fluids to help prevent dehydration caused by diarrhea

Other information

each tbsp. contains: sodium 10 mg
low sodium
sugar free
salicylate 236 mg
protect from freezing
avoid excessive heat (more than 104ºF or 40ºC)
TAMPER EVIDENT: Do not use if imprinted shrink band is missing or broken

Inactive ingredients

Carboxymethylcellulose sodium, flavor, microcrystalline cellulose, potassium hydroxide, potassium sorbate, purified water, red 22, red 28, salicylic acid, simethicone emulsion, sodium benzoate, sucralose, xanthan gum.

Principal Display Panel

Compare to the active ingredient in Pepto-Bismol® Maximum Strength

Pink Bismuth

Maximum Strength

Stomach Relief

Bismuth Subsalicylate 525 mg

Soothing Relief from:

Upset Stomach

Indigestion Nausea

Heartburn

Diarrhea

Original Flavor

FL OZ (mL)

QC SATISFACTION GURANTEED

*This product is not manufactured or distributed by The Procter & Gamble, distributors of Pepto-Bismol®.

Distributed by C.D.M.A., Inc.

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com

Questions: 248-449-9300

QC(CDMA) Maximum Strength Pink Bismuth Subsalicylate525mg

Package Label

QC(CDMA) Maximum Strength Pink Bismuth Subsalicylate525mg

Maximum Strength Stomach Relief

QC STOMACH RELIEF  REGULAR STRENGTH
bismuth subsalicylate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-304
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE, SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE525 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
WATER (UNII: 059QF0KO0R)  
D&C RED NO. 22 (UNII: 1678RKX8RT)  
D&C RED NO. 28 (UNII: 767IP0Y5NH)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorPINK (viscous) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-304-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/16/2019
2NDC:63868-304-12354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/16/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00804/16/2019
Labeler - QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) (011920774)

Revised: 11/2023
Document Id: 36ebec55-11ab-466e-ab52-e5089343eb4d
Set id: 63f191f1-b29f-4842-9d80-ac43117c2361
Version: 4
Effective Time: 20231109
 
QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)