Label: SOOTHE- bismuth subsalicylate liquid
- NDC Code(s): 0363-0025-08, 0363-0025-16
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 10, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each 30 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
- allergic to salicylates (including aspirin)
- taking other salicylate products
Ask a doctor or pharmacist before use if you are
taking any drug for
- diabetes
- gout
- arthritis
- anticoagulation (thinning the blood)
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Directions
- mL = milliliter
- shake well before using
- measure only with dosing cup provided. Do not use any other dosing device
- keep dosing cup with product
- adult and children 12 years and over:
- 30 mL (1 dose) every 1/2 to 1 hour as needed
- do not exceed 8 doses (240 mL)in 24 hour
- use until diarrhea stop but not more than 2 days
- children under 12 years of age: ask a doctor
- drink plenty of clear fluids to help prevent dehydration cause by diarrhea
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to Pepto-Bismal® active ingredient††
Soothe®
BISMUTH SUBSALICYLATE 525 mg /
UPSET STOMACH RELIEVER / ANTIDIARRHEAL
SUGAR FREE
ALCOHOL FREE
- Provides protective coating action to relieve heartburn, indigestion, nausea, upset stomach & diarrhea
CHERRY FLAVOR
FL OZ (mL)
††This product is not manufactured or distributed by Procter & Gamble Company. Pepto-Bismol® is a registered trademark of th Procter & Gamble Company
TAMPER EVIDENT; DO NOT USE IF PRINTED SAFETY SEAL AROUND DOSAGE CUP OR UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD, DEERFIELD.IL 60015
walgreens.com
- Package Label
-
INGREDIENTS AND APPEARANCE
SOOTHE
bismuth subsalicylate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0025 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 30 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) D&C RED NO. 22 (UNII: 1678RKX8RT) D&C RED NO. 28 (UNII: 767IP0Y5NH) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SALICYLIC ACID (UNII: O414PZ4LPZ) SODIUM SALICYLATE (UNII: WIQ1H85SYP) SORBIC ACID (UNII: X045WJ989B) METHYLCELLULOSE (1500 CPS) (UNII: P0NTE48364) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0025-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/31/2015 2 NDC:0363-0025-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/31/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 01/31/2015 Labeler - Walgreens (008965063)