Label: WALGREEN STOMACH RELIEF ULTRA STRENGTH- bismuth subsalicylate suspension
- NDC Code(s): 0363-7071-12
- Packager: WALGREENS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each 15 mL dose)
- Purposes
- 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 or 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
Ask a doctor or pharmacist before use if you are
taking any drug for
- •
- anticoagulation (thinning the blood)
- •
- diabetes
- •
- gout
- •
- arthritis
-
Directions
- •
- shake well before use
- •
- only use dose cup provided
- •
- adults and children 12 years and over:
- •
- 15 mL (1 dose) every ½ hour or 30 mL (2 doses) every hour as needed for diarrhea/traveler’s diarrhea
- •
- 15 mL (1 dose) every ½ hour as needed overindulgence (upset stomach, heartburn, indigestion, nausea)
- •
- do not exceed 8 doses (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
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
NDC 0363-7071-12
*Compare to the active ingredient in Pepto-Bismol® Ultra Strength
Ultra Strength
pink bismuth
bismuth subsalicylate
Upset Stomach Reliever/Antidiarrheal
Natural Cherry flavor
Relieves:
- ▪
- Nausea
- ▪
- Heartburn
- ▪
- Indigestion
- ▪
- Upset Stomach
- ▪
- Diarrhea
12 FL. OZ. (354 mL)
2X CONCENTRATED FORMULA**
Distributed by:
**vs Original Pepto Bismol®
*This product is not manufactured or distributed by Procter & Gamble, distributor of Pepto-Bismol® Ultra Strngth.
-
INGREDIENTS AND APPEARANCE
WALGREEN STOMACH RELIEF ULTRA STRENGTH
bismuth subsalicylate suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7071 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 (UNII: K679OBS311) D&C RED NO. 22 (UNII: 1678RKX8RT) D&C RED NO. 28 (UNII: 767IP0Y5NH) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SALICYLIC ACID (UNII: O414PZ4LPZ) DIMETHICONE, UNSPECIFIED (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:0363-7071-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/16/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 10/16/2023 Labeler - WALGREENS CO. (008965063)