NDC | 63868-304-08, 63868-304-12 |
Set ID | 63f191f1-b29f-4842-9d80-ac43117c2361 |
Category | HUMAN OTC DRUG LABEL |
Packager | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART335 |
- Active ingredient (in each 15 mL)
- Purpose
- Uses
-
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
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- allergic to salicylates (including aspirin)
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- taking other salicylate products
Ask a doctor or pharmacist before use if you are
taking any drug for
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- anticoagulation (thinning the blood)
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- diabetes
- •
- gout
- •
- arthritis
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Directions
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- shake well before use
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- For accurate dosing, use dose cup
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-
adults and children 12 years and over:
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- 1 dose (2 tbsp. or 30 ml) every 1 hour as needed
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- do not exceed 4 doses (8tbsp or 120 mL) in 24 hours
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- 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
- Inactive ingredients
-
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
Questions: 248-449-9300
- Package Label
-
INGREDIENTS AND APPEARANCE
QC STOMACH RELIEF REGULAR STRENGTH
bismuth subsalicylate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-304 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE, SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE 525 mg in 15 mL Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (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 Color PINK (viscous) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-304-08 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/16/2019 2 NDC:63868-304-12 354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/16/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part335 04/16/2019 Labeler - QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) (011920774)