Label: STOMACH RELIEF, 24-7 LIFE- bismuth subsalicylate suspension liquid
STOMACH RELIEF, CASEYS 4GOOD- bismuth subsalicylate suspension liquid
- NDC Code(s): 66715-8355-4, 66715-8554-2
- Packager: Lil' Drug Store Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
Warnings
Reye's syndrome
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
Allergy alert: Contains salicylate. Do not take if you are
- allergic to salicylates (including aspirin)
- taking other salicylate products
Ask a doctor or pharmacist before use if you are
Ask a doctor or pharmacist before use if you are taking any drug for
- anticoagulation (thinning of the blood)
- diabetes
- gout
- arthritis
When using this product
When using this product a temporary, but harmless darkening of the stool and/or tongue may occur
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Directions
Directions
- shake well before use
- mL = milliliter
- TBSP = tablespoon
- measure only with dosing cup provided. Do not use any other dosing device.
- adults and children 12 years and over: 1 dose (2 TBSP or 30 mL) every 1/2 to 1 hour as needed
- do not exceed 8 doses (16 TBSP or 240 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
- Inactive ingredients
- Questions
- Stomach Relief, Casey's 4good PDP/Package
- Stomach Relief, 24/7 Life BY 7-ELEVEN
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INGREDIENTS AND APPEARANCE
STOMACH RELIEF, 24-7 LIFE
bismuth subsalicylate suspension liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-8554 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE 525 mg in 30 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) SACCHARIN SODIUM (UNII: SB8ZUX40TY) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) SALICYLIC ACID (UNII: O414PZ4LPZ) D&C RED NO. 22 (UNII: 1678RKX8RT) D&C RED NO. 28 (UNII: 767IP0Y5NH) BENZOIC ACID (UNII: 8SKN0B0MIM) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) Product Characteristics Color pink Score Shape Size Flavor WINTERGREEN Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-8554-2 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 04/19/2022 STOMACH RELIEF, CASEYS 4GOOD
bismuth subsalicylate suspension liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-8355 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE 525 mg in 30 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) SACCHARIN SODIUM (UNII: SB8ZUX40TY) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) SALICYLIC ACID (UNII: O414PZ4LPZ) D&C RED NO. 22 (UNII: 1678RKX8RT) D&C RED NO. 28 (UNII: 767IP0Y5NH) BENZOIC ACID (UNII: 8SKN0B0MIM) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) Product Characteristics Color pink Score Shape Size Flavor WINTERGREEN Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-8355-4 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 08/01/2023 Labeler - Lil' Drug Store Products, Inc. (093103646)